Canonical Allele Identifier: CA2115203355

Gene: ERCC5 BIVM-ERCC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102846128T= , CM000675.2:g.102846128T=	GRCh38
NC_000013.10:g.103498478T= , CM000675.1:g.103498478T=	GRCh37
NC_000013.9:g.102296479T=	NCBI36
NG_007146.1:g.5305T= , LRG_464:g.5305T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.103T= (ERCC5)
ENST00000682869.1:n.96T= (ERCC5)
ENST00000683246.1:n.224T= (ERCC5)
ENST00000684184.1:n.93T= (ERCC5)
ENST00000638434.1:c.363-7629T= (BIVM-ERCC5)
ENST00000639118.1:c.363-2990T= (BIVM-ERCC5)
ENST00000639132.1:c.764-5990T= (BIVM-ERCC5)	ENSP00000492684.1:n.764-5990T=
ENST00000639435.1:c.1451-5990T= (BIVM-ERCC5)	ENSP00000491742.1:n.1451-5990T=
ENST00000651002.1:c.-139T= (ERCC5)	ENSP00000498809.1:n.-139T=
ENST00000652225.2:c.-139T= (ERCC5) MANE Select	ENSP00000498881.2:n.-139T=
ENST00000652613.1:c.-636T= (ERCC5)	ENSP00000498357.1:n.-636T=
ENST00000355739.8:c.-139T= (ERCC5)	ENSP00000347978.4:n.-139T=
ENST00000375958.3:n.17T= (ERCC5)
ENST00000472151.1:c.-139T= (ERCC5)	ENSP00000436083.1:n.-139T=
ENST00000535557.5:c.-139T= (ERCC5)	ENSP00000442117.1:n.-139T=
ENST00000602836.1:c.1365-5990T= (BIVM-ERCC5)
NM_000123.3:c.-139T= , LRG_464t1:c.-139T= (ERCC5)	NP_000114.2:n.-139T=
NM_001204425.1:c.1451-5990T= (BIVM-ERCC5)	NP_001191354.1:n.1451-5990T=
NM_000123.4:c.-139T= (ERCC5) MANE Select	NP_000114.3:n.-139T=
NM_001204425.2:c.1451-5990T= (BIVM-ERCC5)	NP_001191354.2:n.1451-5990T=