Canonical Allele Identifier: CA1129890599
Gene: COL5A1 HGNC NCBI

Linked Data

dbSNP Id: rs1839033482

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134822185A>T , CM000671.2:g.134822185A>T GRCh38
NC_000009.11:g.137714031A>T , CM000671.1:g.137714031A>T GRCh37
NC_000009.10:g.136853852A>T NCBI36
NG_008030.1:g.185380A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371820.4:c.4608+35A>T ENSP00000360885.4:n.4608+35A>T
ENST00000371817.8:c.4608+35A>T MANE Select ENSP00000360882.3:n.4608+35A>T
ENST00000371817.7:c.4608+35A>T ENSP00000360882.3:n.4608+35A>T
ENST00000618395.4:c.4608+35A>T ENSP00000481360.1:n.4608+35A>T
NM_000093.4:c.4608+35A>T NP_000084.3:n.4608+35A>T
NM_001278074.1:c.4608+35A>T NP_001265003.1:n.4608+35A>T
NR_103451.2:n.71-1976T>A
XR_929712.1:n.5010+35A>T
XR_929713.1:n.5010+35A>T
XM_017014266.2:c.4608+35A>T XP_016869755.1:n.4608+35A>T
XR_001746183.1:n.5006+35A>T
NM_000093.5:c.4608+35A>T MANE Select NP_000084.3:n.4608+35A>T