Canonical Allele Identifier: CA375460730
Gene: COL5A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2006814
ClinVar RCV Id: RCV002837925
dbSNP Id: rs1281200207

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134835122C>T , CM000671.2:g.134835122C>T GRCh38
NC_000009.11:g.137726968C>T , CM000671.1:g.137726968C>T GRCh37
NC_000009.10:g.136866789C>T NCBI36
NG_008030.1:g.198317C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371820.4:c.5288C>T ENSP00000360885.4:p.Ala1763Val
ENST00000371817.8:c.5288C>T MANE Select ENSP00000360882.3:p.Ala1763Val
ENST00000371817.7:c.5288C>T ENSP00000360882.3:p.Ala1763Val
ENST00000371820.3:c.546C>T
ENST00000618395.4:c.5288C>T ENSP00000481360.1:p.Ala1763Val
NM_000093.4:c.5288C>T NP_000084.3:p.Ala1763Val
NM_001278074.1:c.5288C>T NP_001265003.1:p.Ala1763Val
NR_103451.2:n.71-14913G>A
NM_000093.5:c.5288C>T MANE Select NP_000084.3:p.Ala1763Val