Canonical Allele Identifier: CA484776105

Gene: ERCC5 BIVM-ERCC5

Linked Data

• dbSNP Id: rs2140517243
• MyVariant Identifiers: chr13:g.103504502A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102852152A>G , CM000675.2:g.102852152A>G	GRCh38
NC_000013.10:g.103504502A>G , CM000675.1:g.103504502A>G	GRCh37
NC_000013.9:g.102302503A>G	NCBI36
NG_007146.1:g.11329A>G , LRG_464:g.11329A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.364A>G (ERCC5)
ENST00000682869.1:n.357A>G (ERCC5)
ENST00000683246.1:n.485A>G (ERCC5)
ENST00000684184.1:n.354A>G (ERCC5)
ENST00000638434.1:c.363-1605A>G (BIVM-ERCC5)
ENST00000639118.1:c.474A>G (BIVM-ERCC5)
ENST00000639132.1:c.798A>G (BIVM-ERCC5)	ENSP00000492684.1:p.Gly266=
ENST00000639435.1:c.1485A>G (BIVM-ERCC5)	ENSP00000491742.1:p.Gly495=
ENST00000651002.1:c.123A>G (ERCC5)	ENSP00000498809.1:p.Gly41=
ENST00000651055.1:n.252A>G (ERCC5)
ENST00000651281.1:n.491A>G (ERCC5)
ENST00000651470.1:c.123A>G (ERCC5)	ENSP00000498701.1:p.Gly41=
ENST00000652225.2:c.123A>G (ERCC5) MANE Select	ENSP00000498881.2:p.Gly41=
ENST00000652613.1:c.-382A>G (ERCC5)	ENSP00000498357.1:n.-382A>G
ENST00000355739.8:c.123A>G (ERCC5)	ENSP00000347978.4:p.Gly41=
ENST00000375958.3:n.278A>G (ERCC5)
ENST00000472151.1:c.*28A>G (ERCC5)	ENSP00000436083.1:n.*28A>G
ENST00000535557.5:c.123A>G (ERCC5)	ENSP00000442117.1:p.Gly41=
ENST00000602836.1:c.1399A>G (BIVM-ERCC5)
ENST00000610537.4:c.123A>G (ERCC5)	ENSP00000478667.1:p.Gly41=
NM_000123.3:c.123A>G , LRG_464t1:c.123A>G (ERCC5)	NP_000114.2:p.Gly41=
NM_001204425.1:c.1485A>G (BIVM-ERCC5)	NP_001191354.1:p.Gly495=
NM_000123.4:c.123A>G (ERCC5) MANE Select	NP_000114.3:p.Gly41=
NM_001204425.2:c.1485A>G (BIVM-ERCC5)	NP_001191354.2:p.Gly495=