Canonical Allele Identifier: CA388673553

Gene: ERCC5 BIVM-ERCC5

Linked Data

• MyVariant Identifiers: chr13:g.103525661T>G (hg19) ; chr13:g.102873311T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102873311T>G , CM000675.2:g.102873311T>G	GRCh38
NC_000013.10:g.103525661T>G , CM000675.1:g.103525661T>G	GRCh37
NC_000013.9:g.102323662T>G	NCBI36
NG_007146.1:g.32488T>G , LRG_464:g.32488T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.4033T>G (ERCC5)
ENST00000682869.1:n.3581T>G (ERCC5)
ENST00000683246.1:n.4569T>G (ERCC5)
ENST00000683642.1:n.3162T>G (ERCC5)
ENST00000639132.1:c.3607T>G (BIVM-ERCC5)	ENSP00000492684.1:p.Phe1203Val
ENST00000639435.1:c.4294T>G (BIVM-ERCC5)	ENSP00000491742.1:p.Phe1432Val
ENST00000651002.1:c.*2693T>G (ERCC5)	ENSP00000498809.1:n.*2693T>G
ENST00000651055.1:n.3059T>G (ERCC5)
ENST00000651281.1:n.3300T>G (ERCC5)
ENST00000651387.1:n.2416T>G (ERCC5)
ENST00000651470.1:c.*104T>G (ERCC5)	ENSP00000498701.1:n.*104T>G
ENST00000652225.2:c.2932T>G (ERCC5) MANE Select	ENSP00000498881.2:p.Phe978Val
ENST00000652613.1:c.2428T>G (ERCC5)	ENSP00000498357.1:p.Phe810Val
ENST00000355739.8:c.2932T>G (ERCC5)	ENSP00000347978.4:p.Phe978Val
ENST00000375954.1:c.631T>G (ERCC5)	ENSP00000365121.1:p.Phe211Val
ENST00000610537.4:c.2929T>G (ERCC5)	ENSP00000478667.1:p.Phe977Val
NM_000123.3:c.2932T>G , LRG_464t1:c.2932T>G (ERCC5)	NP_000114.2:p.Phe978Val
NM_001204425.1:c.4294T>G (BIVM-ERCC5)	NP_001191354.1:p.Phe1432Val
NM_000123.4:c.2932T>G (ERCC5) MANE Select	NP_000114.3:p.Phe978Val
NM_001204425.2:c.4294T>G (BIVM-ERCC5)	NP_001191354.2:p.Phe1432Val