Canonical Allele Identifier: CA2115203354
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102846127G= , CM000675.2:g.102846127G= GRCh38
NC_000013.10:g.103498477G= , CM000675.1:g.103498477G= GRCh37
NC_000013.9:g.102296478G= NCBI36
NG_007146.1:g.5304G= , LRG_464:g.5304G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.102G= (ERCC5)
ENST00000682869.1:n.95G= (ERCC5)
ENST00000683246.1:n.223G= (ERCC5)
ENST00000684184.1:n.92G= (ERCC5)
ENST00000638434.1:c.363-7630G= (BIVM-ERCC5)
ENST00000639118.1:c.363-2991G= (BIVM-ERCC5)
ENST00000639132.1:c.764-5991G= (BIVM-ERCC5) ENSP00000492684.1:n.764-5991G=
ENST00000639435.1:c.1451-5991G= (BIVM-ERCC5) ENSP00000491742.1:n.1451-5991G=
ENST00000651002.1:c.-140G= (ERCC5) ENSP00000498809.1:n.-140G=
ENST00000652225.2:c.-140G= (ERCC5) MANE Select ENSP00000498881.2:n.-140G=
ENST00000652613.1:c.-637G= (ERCC5) ENSP00000498357.1:n.-637G=
ENST00000355739.8:c.-140G= (ERCC5) ENSP00000347978.4:n.-140G=
ENST00000375958.3:n.16G= (ERCC5)
ENST00000472151.1:c.-140G= (ERCC5) ENSP00000436083.1:n.-140G=
ENST00000535557.5:c.-140G= (ERCC5) ENSP00000442117.1:n.-140G=
ENST00000602836.1:c.1365-5991G= (BIVM-ERCC5)
NM_000123.3:c.-140G= , LRG_464t1:c.-140G= (ERCC5) NP_000114.2:n.-140G=
NM_001204425.1:c.1451-5991G= (BIVM-ERCC5) NP_001191354.1:n.1451-5991G=
NM_000123.4:c.-140G= (ERCC5) MANE Select NP_000114.3:n.-140G=
NM_001204425.2:c.1451-5991G= (BIVM-ERCC5) NP_001191354.2:n.1451-5991G=