Canonical Allele Identifier: CA484859218

Gene: ERCC5 BIVM-ERCC5

Linked Data

• MyVariant Identifiers: chr13:g.103525657T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102873307T>G , CM000675.2:g.102873307T>G	GRCh38
NC_000013.10:g.103525657T>G , CM000675.1:g.103525657T>G	GRCh37
NC_000013.9:g.102323658T>G	NCBI36
NG_007146.1:g.32484T>G , LRG_464:g.32484T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.4029T>G (ERCC5)
ENST00000682869.1:n.3577T>G (ERCC5)
ENST00000683246.1:n.4565T>G (ERCC5)
ENST00000683642.1:n.3158T>G (ERCC5)
ENST00000639132.1:c.3603T>G (BIVM-ERCC5)	ENSP00000492684.1:p.Ser1201=
ENST00000639435.1:c.4290T>G (BIVM-ERCC5)	ENSP00000491742.1:p.Ser1430=
ENST00000651002.1:c.*2689T>G (ERCC5)	ENSP00000498809.1:n.*2689T>G
ENST00000651055.1:n.3055T>G (ERCC5)
ENST00000651281.1:n.3296T>G (ERCC5)
ENST00000651387.1:n.2412T>G (ERCC5)
ENST00000651470.1:c.*100T>G (ERCC5)	ENSP00000498701.1:n.*100T>G
ENST00000652225.2:c.2928T>G (ERCC5) MANE Select	ENSP00000498881.2:p.Ser976=
ENST00000652613.1:c.2424T>G (ERCC5)	ENSP00000498357.1:p.Ser808=
ENST00000355739.8:c.2928T>G (ERCC5)	ENSP00000347978.4:p.Ser976=
ENST00000375954.1:c.627T>G (ERCC5)	ENSP00000365121.1:p.Ser209=
ENST00000610537.4:c.2925T>G (ERCC5)	ENSP00000478667.1:p.Ser975=
NM_000123.3:c.2928T>G , LRG_464t1:c.2928T>G (ERCC5)	NP_000114.2:p.Ser976=
NM_001204425.1:c.4290T>G (BIVM-ERCC5)	NP_001191354.1:p.Ser1430=
NM_000123.4:c.2928T>G (ERCC5) MANE Select	NP_000114.3:p.Ser976=
NM_001204425.2:c.4290T>G (BIVM-ERCC5)	NP_001191354.2:p.Ser1430=