Canonical Allele Identifier: CA388675078
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875643T>G , CM000675.2:g.102875643T>G GRCh38
NC_000013.10:g.103527993T>G , CM000675.1:g.103527993T>G GRCh37
NC_000013.9:g.102325994T>G NCBI36
NG_007146.1:g.34820T>G , LRG_464:g.34820T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4402T>G (ERCC5)
ENST00000682869.1:n.3950T>G (ERCC5)
ENST00000683246.1:n.4938T>G (ERCC5)
ENST00000683642.1:n.3531T>G (ERCC5)
ENST00000639132.1:c.3976T>G (BIVM-ERCC5) ENSP00000492684.1:p.Ser1326Ala
ENST00000639435.1:c.4663T>G (BIVM-ERCC5) ENSP00000491742.1:p.Ser1555Ala
ENST00000651002.1:c.*3062T>G (ERCC5) ENSP00000498809.1:n.*3062T>G
ENST00000651055.1:n.3428T>G (ERCC5)
ENST00000651281.1:n.3669T>G (ERCC5)
ENST00000651387.1:n.2785T>G (ERCC5)
ENST00000651470.1:c.*473T>G (ERCC5) ENSP00000498701.1:n.*473T>G
ENST00000652225.2:c.3301T>G (ERCC5) MANE Select ENSP00000498881.2:p.Ser1101Ala
ENST00000652613.1:c.2797T>G (ERCC5) ENSP00000498357.1:p.Ser933Ala
ENST00000355739.8:c.3301T>G (ERCC5) ENSP00000347978.4:p.Ser1101Ala
ENST00000375954.1:c.1000T>G (ERCC5) ENSP00000365121.1:p.Ser334Ala
ENST00000472247.1:n.461T>G (ERCC5)
ENST00000610537.4:c.3298T>G (ERCC5) ENSP00000478667.1:p.Ser1100Ala
NM_000123.3:c.3301T>G , LRG_464t1:c.3301T>G (ERCC5) NP_000114.2:p.Ser1101Ala
NM_001204425.1:c.4663T>G (BIVM-ERCC5) NP_001191354.1:p.Ser1555Ala
NM_000123.4:c.3301T>G (ERCC5) MANE Select NP_000114.3:p.Ser1101Ala
NM_001204425.2:c.4663T>G (BIVM-ERCC5) NP_001191354.2:p.Ser1555Ala