Canonical Allele Identifier: CA388674913

Gene: ERCC5 BIVM-ERCC5

Linked Data

• MyVariant Identifiers: chr13:g.103527913G>T (hg19) ; chr13:g.102875563G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102875563G>T , CM000675.2:g.102875563G>T	GRCh38
NC_000013.10:g.103527913G>T , CM000675.1:g.103527913G>T	GRCh37
NC_000013.9:g.102325914G>T	NCBI36
NG_007146.1:g.34740G>T , LRG_464:g.34740G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682632.1:n.4322G>T (ERCC5)
ENST00000682869.1:n.3870G>T (ERCC5)
ENST00000683246.1:n.4858G>T (ERCC5)
ENST00000683642.1:n.3451G>T (ERCC5)
ENST00000639132.1:c.3896G>T (BIVM-ERCC5)	ENSP00000492684.1:p.Arg1299Met
ENST00000639435.1:c.4583G>T (BIVM-ERCC5)	ENSP00000491742.1:p.Arg1528Met
ENST00000651002.1:c.*2982G>T (ERCC5)	ENSP00000498809.1:n.*2982G>T
ENST00000651055.1:n.3348G>T (ERCC5)
ENST00000651281.1:n.3589G>T (ERCC5)
ENST00000651387.1:n.2705G>T (ERCC5)
ENST00000651470.1:c.*393G>T (ERCC5)	ENSP00000498701.1:n.*393G>T
ENST00000652225.2:c.3221G>T (ERCC5) MANE Select	ENSP00000498881.2:p.Arg1074Met
ENST00000652613.1:c.2717G>T (ERCC5)	ENSP00000498357.1:p.Arg906Met
ENST00000355739.8:c.3221G>T (ERCC5)	ENSP00000347978.4:p.Arg1074Met
ENST00000375954.1:c.920G>T (ERCC5)	ENSP00000365121.1:p.Arg307Met
ENST00000472247.1:n.381G>T (ERCC5)
ENST00000610537.4:c.3218G>T (ERCC5)	ENSP00000478667.1:p.Arg1073Met
NM_000123.3:c.3221G>T , LRG_464t1:c.3221G>T (ERCC5)	NP_000114.2:p.Arg1074Met
NM_001204425.1:c.4583G>T (BIVM-ERCC5)	NP_001191354.1:p.Arg1528Met
NM_000123.4:c.3221G>T (ERCC5) MANE Select	NP_000114.3:p.Arg1074Met
NM_001204425.2:c.4583G>T (BIVM-ERCC5)	NP_001191354.2:p.Arg1528Met