Canonical Allele Identifier: CA484777018

Gene: ERCC5 BIVM-ERCC5

Linked Data

• MyVariant Identifiers: chr13:g.103515278T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102862928T>A , CM000675.2:g.102862928T>A	GRCh38
NC_000013.10:g.103515278T>A , CM000675.1:g.103515278T>A	GRCh37
NC_000013.9:g.102313279T>A	NCBI36
NG_007146.1:g.22105T>A , LRG_464:g.22105T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.2020T>A (ERCC5)
ENST00000682869.1:n.2428T>A (ERCC5)
ENST00000683246.1:n.2556T>A (ERCC5)
ENST00000639132.1:c.2454T>A (BIVM-ERCC5)	ENSP00000492684.1:p.Pro818=
ENST00000639435.1:c.3141T>A (BIVM-ERCC5)	ENSP00000491742.1:p.Pro1047=
ENST00000651002.1:c.*1540T>A (ERCC5)	ENSP00000498809.1:n.*1540T>A
ENST00000651055.1:n.1908T>A (ERCC5)
ENST00000651281.1:n.2147T>A (ERCC5)
ENST00000651387.1:n.1263T>A (ERCC5)
ENST00000651470.1:c.1779T>A (ERCC5)	ENSP00000498701.1:p.Pro593=
ENST00000652225.2:c.1779T>A (ERCC5) MANE Select	ENSP00000498881.2:p.Pro593=
ENST00000652613.1:c.1275T>A (ERCC5)	ENSP00000498357.1:p.Pro425=
ENST00000355739.8:c.1779T>A (ERCC5)	ENSP00000347978.4:p.Pro593=
ENST00000602836.1:c.3055T>A (BIVM-ERCC5)
ENST00000610537.4:c.1779T>A (ERCC5)	ENSP00000478667.1:p.Pro593=
NM_000123.3:c.1779T>A , LRG_464t1:c.1779T>A (ERCC5)	NP_000114.2:p.Pro593=
NM_001204425.1:c.3141T>A (BIVM-ERCC5)	NP_001191354.1:p.Pro1047=
NM_000123.4:c.1779T>A (ERCC5) MANE Select	NP_000114.3:p.Pro593=
NM_001204425.2:c.3141T>A (BIVM-ERCC5)	NP_001191354.2:p.Pro1047=