Canonical Allele Identifier: CA2115215338

Gene: ERCC5 BIVM-ERCC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102873291C= , CM000675.2:g.102873291C=	GRCh38
NC_000013.10:g.103525641C= , CM000675.1:g.103525641C=	GRCh37
NC_000013.9:g.102323642C=	NCBI36
NG_007146.1:g.32468C= , LRG_464:g.32468C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682632.1:n.4013C= (ERCC5)
ENST00000682869.1:n.3561C= (ERCC5)
ENST00000683246.1:n.4549C= (ERCC5)
ENST00000683642.1:n.3142C= (ERCC5)
ENST00000639132.1:c.3587C= (BIVM-ERCC5)	ENSP00000492684.1:p.Thr1196=
ENST00000639435.1:c.4274C= (BIVM-ERCC5)	ENSP00000491742.1:p.Thr1425=
ENST00000651002.1:c.*2673C= (ERCC5)	ENSP00000498809.1:n.*2673C=
ENST00000651055.1:n.3039C= (ERCC5)
ENST00000651281.1:n.3280C= (ERCC5)
ENST00000651387.1:n.2396C= (ERCC5)
ENST00000651470.1:c.*84C= (ERCC5)	ENSP00000498701.1:n.*84C=
ENST00000652225.2:c.2912C= (ERCC5) MANE Select	ENSP00000498881.2:p.Thr971=
ENST00000652613.1:c.2408C= (ERCC5)	ENSP00000498357.1:p.Thr803=
ENST00000355739.8:c.2912C= (ERCC5)	ENSP00000347978.4:p.Thr971=
ENST00000375954.1:c.611C= (ERCC5)	ENSP00000365121.1:p.Thr204=
ENST00000610537.4:c.2909C= (ERCC5)	ENSP00000478667.1:p.Thr970=
NM_000123.3:c.2912C= , LRG_464t1:c.2912C= (ERCC5)	NP_000114.2:p.Thr971=
NM_001204425.1:c.4274C= (BIVM-ERCC5)	NP_001191354.1:p.Thr1425=
NM_000123.4:c.2912C= (ERCC5) MANE Select	NP_000114.3:p.Thr971=
NM_001204425.2:c.4274C= (BIVM-ERCC5)	NP_001191354.2:p.Thr1425=