Canonical Allele Identifier: CA10626800
Community Standard Title: NM_000093.5(COL5A1):c.3939G>T (p.Glu1313Asp)
Gene: COL5A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134814829G>T , CM000671.2:g.134814829G>T GRCh38
NC_000009.11:g.137706675G>T , CM000671.1:g.137706675G>T GRCh37
NC_000009.10:g.136846496G>T NCBI36
NG_008030.1:g.178024G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000093.5:c.3939G>T MANE Select NP_000084.3:p.Glu1313Asp
ENST00000371817.8:c.3939G>T MANE Select ENSP00000360882.3:p.Glu1313Asp
NM_000093.4:c.3939G>T NP_000084.3:p.Glu1313Asp
NM_001278074.1:c.3939G>T NP_001265003.1:p.Glu1313Asp
ENST00000371817.7:c.3939G>T ENSP00000360882.3:p.Glu1313Asp
ENST00000371820.4:c.3939G>T ENSP00000360885.4:p.Glu1313Asp
ENST00000618395.4:c.3939G>T ENSP00000481360.1:p.Glu1313Asp
XM_017014266.2:c.3939G>T XP_016869755.1:p.Glu1313Asp
XR_001746183.1:n.4337G>T
XR_929712.1:n.4341G>T
XR_929713.1:n.4341G>T