Canonical Allele Identifier: CA2115208014

Gene: ERCC5 BIVM-ERCC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102856086A= , CM000675.2:g.102856086A=	GRCh38
NC_000013.10:g.103508436A= , CM000675.1:g.103508436A=	GRCh37
NC_000013.9:g.102306437A=	NCBI36
NG_007146.1:g.15263A= , LRG_464:g.15263A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.743A= (ERCC5)
ENST00000682869.1:n.1151A= (ERCC5)
ENST00000683246.1:n.1279A= (ERCC5)
ENST00000684184.1:n.1148A= (ERCC5)
ENST00000638434.1:c.600A= (BIVM-ERCC5)
ENST00000639132.1:c.1177A= (BIVM-ERCC5)	ENSP00000492684.1:p.Arg393=
ENST00000639435.1:c.1864A= (BIVM-ERCC5)	ENSP00000491742.1:p.Arg622=
ENST00000651002.1:c.*263A= (ERCC5)	ENSP00000498809.1:n.*263A=
ENST00000651055.1:n.631A= (ERCC5)
ENST00000651281.1:n.870A= (ERCC5)
ENST00000651470.1:c.502A= (ERCC5)	ENSP00000498701.1:p.Arg168=
ENST00000652225.2:c.502A= (ERCC5) MANE Select	ENSP00000498881.2:p.Arg168=
ENST00000652613.1:c.-3A= (ERCC5)	ENSP00000498357.1:n.-3A=
ENST00000355739.8:c.502A= (ERCC5)	ENSP00000347978.4:p.Arg168=
ENST00000535557.5:c.502A= (ERCC5)	ENSP00000442117.1:p.Arg168=
ENST00000602836.1:c.1778A= (BIVM-ERCC5)
ENST00000610537.4:c.502A= (ERCC5)	ENSP00000478667.1:p.Arg168=
NM_000123.3:c.502A= , LRG_464t1:c.502A= (ERCC5)	NP_000114.2:p.Arg168=
NM_001204425.1:c.1864A= (BIVM-ERCC5)	NP_001191354.1:p.Arg622=
NM_000123.4:c.502A= (ERCC5) MANE Select	NP_000114.3:p.Arg168=
NM_001204425.2:c.1864A= (BIVM-ERCC5)	NP_001191354.2:p.Arg622=