Canonical Allele Identifier: CA2115216493
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875608G= , CM000675.2:g.102875608G= GRCh38
NC_000013.10:g.103527958G= , CM000675.1:g.103527958G= GRCh37
NC_000013.9:g.102325959G= NCBI36
NG_007146.1:g.34785G= , LRG_464:g.34785G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4367G= (ERCC5)
ENST00000682869.1:n.3915G= (ERCC5)
ENST00000683246.1:n.4903G= (ERCC5)
ENST00000683642.1:n.3496G= (ERCC5)
ENST00000639132.1:c.3941G= (BIVM-ERCC5) ENSP00000492684.1:p.Gly1314=
ENST00000639435.1:c.4628G= (BIVM-ERCC5) ENSP00000491742.1:p.Gly1543=
ENST00000651002.1:c.*3027G= (ERCC5) ENSP00000498809.1:n.*3027G=
ENST00000651055.1:n.3393G= (ERCC5)
ENST00000651281.1:n.3634G= (ERCC5)
ENST00000651387.1:n.2750G= (ERCC5)
ENST00000651470.1:c.*438G= (ERCC5) ENSP00000498701.1:n.*438G=
ENST00000652225.2:c.3266G= (ERCC5) MANE Select ENSP00000498881.2:p.Gly1089=
ENST00000652613.1:c.2762G= (ERCC5) ENSP00000498357.1:p.Gly921=
ENST00000355739.8:c.3266G= (ERCC5) ENSP00000347978.4:p.Gly1089=
ENST00000375954.1:c.965G= (ERCC5) ENSP00000365121.1:p.Gly322=
ENST00000472247.1:n.426G= (ERCC5)
ENST00000610537.4:c.3263G= (ERCC5) ENSP00000478667.1:p.Gly1088=
NM_000123.3:c.3266G= , LRG_464t1:c.3266G= (ERCC5) NP_000114.2:p.Gly1089=
NM_001204425.1:c.4628G= (BIVM-ERCC5) NP_001191354.1:p.Gly1543=
NM_000123.4:c.3266G= (ERCC5) MANE Select NP_000114.3:p.Gly1089=
NM_001204425.2:c.4628G= (BIVM-ERCC5) NP_001191354.2:p.Gly1543=