Canonical Allele Identifier: CA2115215330

Gene: ERCC5 BIVM-ERCC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102873277C= , CM000675.2:g.102873277C=	GRCh38
NC_000013.10:g.103525627C= , CM000675.1:g.103525627C=	GRCh37
NC_000013.9:g.102323628C=	NCBI36
NG_007146.1:g.32454C= , LRG_464:g.32454C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.3999C= (ERCC5)
ENST00000682869.1:n.3547C= (ERCC5)
ENST00000683246.1:n.4535C= (ERCC5)
ENST00000683642.1:n.3128C= (ERCC5)
ENST00000639132.1:c.3573C= (BIVM-ERCC5)	ENSP00000492684.1:p.Phe1191=
ENST00000639435.1:c.4260C= (BIVM-ERCC5)	ENSP00000491742.1:p.Phe1420=
ENST00000651002.1:c.*2659C= (ERCC5)	ENSP00000498809.1:n.*2659C=
ENST00000651055.1:n.3025C= (ERCC5)
ENST00000651281.1:n.3266C= (ERCC5)
ENST00000651387.1:n.2382C= (ERCC5)
ENST00000651470.1:c.*70C= (ERCC5)	ENSP00000498701.1:n.*70C=
ENST00000652225.2:c.2898C= (ERCC5) MANE Select	ENSP00000498881.2:p.Phe966=
ENST00000652613.1:c.2394C= (ERCC5)	ENSP00000498357.1:p.Phe798=
ENST00000355739.8:c.2898C= (ERCC5)	ENSP00000347978.4:p.Phe966=
ENST00000375954.1:c.597C= (ERCC5)	ENSP00000365121.1:p.Phe199=
ENST00000610537.4:c.2895C= (ERCC5)	ENSP00000478667.1:p.Phe965=
NM_000123.3:c.2898C= , LRG_464t1:c.2898C= (ERCC5)	NP_000114.2:p.Phe966=
NM_001204425.1:c.4260C= (BIVM-ERCC5)	NP_001191354.1:p.Phe1420=
NM_000123.4:c.2898C= (ERCC5) MANE Select	NP_000114.3:p.Phe966=
NM_001204425.2:c.4260C= (BIVM-ERCC5)	NP_001191354.2:p.Phe1420=