Version: 8.0.0
Date: Tue Jan 28 2025
13 results for calc1

calca

(Xenopus tropicalis)
Gene
Name: calcitonin-related polypeptide alpha
Synonyms: calcitonin-related polypeptide alpha, calcitonin, LOC108715309, LOC108713444, calca, cgrp, cgrp1, calc1, cgrp-i
Source: Xenbase:XB-GENE-6461042
Biotype: gene
Synonyms: calc1...calc1...calc1

CALCA

(Homo sapiens)
Gene
Name: calcitonin related polypeptide alpha
Synonyms: PCT, calcitonin-related polypeptide alpha, katacalcin, calcitonin, CGRP-alpha, calcitonin gene-related peptide I, MGC126648, alpha-type CGRP, CT, calcitonin gene-related peptide 1, calcitonin 1, CALC1, KC, CGRP, CGRP-I, calcitonin/calcitonin-related polypeptide, alpha, CGRP1
Source: HGNC:1437
Biotype: protein coding gene
Synonyms: CALC1...CALC1

(GRCh38)11:14967805G>A

(Homo sapiens)
Allele/Variant
Source: rs782816793
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14967805G>A
Gene Synonyms: CALC1

(GRCh38)11:14970040G>A

(Homo sapiens)
Allele/Variant
Source: rs147263808
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14970040G>A
Gene Synonyms: CALC1

(GRCh38)11:14968891C>A

(Homo sapiens)
Allele/Variant
Source: rs34670162
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14968891C>A
Gene Synonyms: CALC1

(GRCh38)11:14967804C>T

(Homo sapiens)
Allele/Variant
Source: rs782028430
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14967804C>T
Gene Synonyms: CALC1

(GRCh38)11:14968847C>T

(Homo sapiens)
Allele/Variant
Source: rs35425520
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14968847C>T
Gene Synonyms: CALC1

(GRCh38)11:14967707G>T

(Homo sapiens)
Allele/Variant
Source: rs781977175
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14967707G>T
Gene Synonyms: CALC1

(GRCh38)11:14968907G>A

(Homo sapiens)
Allele/Variant
Source: rs142242325
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14968907G>A
Gene Synonyms: CALC1

(GRCh38)11:14967715G>A

(Homo sapiens)
Allele/Variant
Source: rs782436716
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14967715G>A
Gene Synonyms: CALC1

(GRCh38)11:14967810G>T

(Homo sapiens)
Allele/Variant
Source: rs1376969693
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14967810G>T
Gene Synonyms: CALC1

(GRCh38)11:14971141A>T

(Homo sapiens)
Allele/Variant
Source: rs144571175
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14971141A>T
Gene Synonyms: CALC1

(GRCh38)11:14971162C>T

(Homo sapiens)
Allele/Variant
Source: rs1555026441
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14971162C>T
Gene Synonyms: CALC1