Canonical Allele Identifier: CA484968563
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.103515254A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102862904A>G , CM000675.2:g.102862904A>G GRCh38
NC_000013.10:g.103515254A>G , CM000675.1:g.103515254A>G GRCh37
NC_000013.9:g.102313255A>G NCBI36
NG_007146.1:g.22081A>G , LRG_464:g.22081A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.1996A>G (ERCC5)
ENST00000682869.1:n.2404A>G (ERCC5)
ENST00000683246.1:n.2532A>G (ERCC5)
ENST00000639132.1:c.2430A>G (BIVM-ERCC5) ENSP00000492684.1:p.Glu810=
ENST00000639435.1:c.3117A>G (BIVM-ERCC5) ENSP00000491742.1:p.Glu1039=
ENST00000651002.1:c.*1516A>G (ERCC5) ENSP00000498809.1:n.*1516A>G
ENST00000651055.1:n.1884A>G (ERCC5)
ENST00000651281.1:n.2123A>G (ERCC5)
ENST00000651387.1:n.1239A>G (ERCC5)
ENST00000651470.1:c.1755A>G (ERCC5) ENSP00000498701.1:p.Glu585=
ENST00000652225.2:c.1755A>G (ERCC5) MANE Select ENSP00000498881.2:p.Glu585=
ENST00000652613.1:c.1251A>G (ERCC5) ENSP00000498357.1:p.Glu417=
ENST00000355739.8:c.1755A>G (ERCC5) ENSP00000347978.4:p.Glu585=
ENST00000602836.1:c.3031A>G (BIVM-ERCC5)
ENST00000610537.4:c.1755A>G (ERCC5) ENSP00000478667.1:p.Glu585=
NM_000123.3:c.1755A>G , LRG_464t1:c.1755A>G (ERCC5) NP_000114.2:p.Glu585=
NM_001204425.1:c.3117A>G (BIVM-ERCC5) NP_001191354.1:p.Glu1039=
NM_000123.4:c.1755A>G (ERCC5) MANE Select NP_000114.3:p.Glu585=
NM_001204425.2:c.3117A>G (BIVM-ERCC5) NP_001191354.2:p.Glu1039=