Canonical Allele Identifier: CA2115216499

Gene: ERCC5 BIVM-ERCC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102875614C= , CM000675.2:g.102875614C=	GRCh38
NC_000013.10:g.103527964C= , CM000675.1:g.103527964C=	GRCh37
NC_000013.9:g.102325965C=	NCBI36
NG_007146.1:g.34791C= , LRG_464:g.34791C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.4373C= (ERCC5)
ENST00000682869.1:n.3921C= (ERCC5)
ENST00000683246.1:n.4909C= (ERCC5)
ENST00000683642.1:n.3502C= (ERCC5)
ENST00000639132.1:c.3947C= (BIVM-ERCC5)	ENSP00000492684.1:p.Thr1316=
ENST00000639435.1:c.4634C= (BIVM-ERCC5)	ENSP00000491742.1:p.Thr1545=
ENST00000651002.1:c.*3033C= (ERCC5)	ENSP00000498809.1:n.*3033C=
ENST00000651055.1:n.3399C= (ERCC5)
ENST00000651281.1:n.3640C= (ERCC5)
ENST00000651387.1:n.2756C= (ERCC5)
ENST00000651470.1:c.*444C= (ERCC5)	ENSP00000498701.1:n.*444C=
ENST00000652225.2:c.3272C= (ERCC5) MANE Select	ENSP00000498881.2:p.Thr1091=
ENST00000652613.1:c.2768C= (ERCC5)	ENSP00000498357.1:p.Thr923=
ENST00000355739.8:c.3272C= (ERCC5)	ENSP00000347978.4:p.Thr1091=
ENST00000375954.1:c.971C= (ERCC5)	ENSP00000365121.1:p.Thr324=
ENST00000472247.1:n.432C= (ERCC5)
ENST00000610537.4:c.3269C= (ERCC5)	ENSP00000478667.1:p.Thr1090=
NM_000123.3:c.3272C= , LRG_464t1:c.3272C= (ERCC5)	NP_000114.2:p.Thr1091=
NM_001204425.1:c.4634C= (BIVM-ERCC5)	NP_001191354.1:p.Thr1545=
NM_000123.4:c.3272C= (ERCC5) MANE Select	NP_000114.3:p.Thr1091=
NM_001204425.2:c.4634C= (BIVM-ERCC5)	NP_001191354.2:p.Thr1545=