Canonical Allele Identifier: CA388674889
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875554A>C , CM000675.2:g.102875554A>C GRCh38
NC_000013.10:g.103527904A>C , CM000675.1:g.103527904A>C GRCh37
NC_000013.9:g.102325905A>C NCBI36
NG_007146.1:g.34731A>C , LRG_464:g.34731A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682632.1:n.4313A>C (ERCC5)
ENST00000682869.1:n.3861A>C (ERCC5)
ENST00000683246.1:n.4849A>C (ERCC5)
ENST00000683642.1:n.3442A>C (ERCC5)
ENST00000639132.1:c.3887A>C (BIVM-ERCC5) ENSP00000492684.1:p.Lys1296Thr
ENST00000639435.1:c.4574A>C (BIVM-ERCC5) ENSP00000491742.1:p.Lys1525Thr
ENST00000651002.1:c.*2973A>C (ERCC5) ENSP00000498809.1:n.*2973A>C
ENST00000651055.1:n.3339A>C (ERCC5)
ENST00000651281.1:n.3580A>C (ERCC5)
ENST00000651387.1:n.2696A>C (ERCC5)
ENST00000651470.1:c.*384A>C (ERCC5) ENSP00000498701.1:n.*384A>C
ENST00000652225.2:c.3212A>C (ERCC5) MANE Select ENSP00000498881.2:p.Lys1071Thr
ENST00000652613.1:c.2708A>C (ERCC5) ENSP00000498357.1:p.Lys903Thr
ENST00000355739.8:c.3212A>C (ERCC5) ENSP00000347978.4:p.Lys1071Thr
ENST00000375954.1:c.911A>C (ERCC5) ENSP00000365121.1:p.Lys304Thr
ENST00000472247.1:n.372A>C (ERCC5)
ENST00000610537.4:c.3209A>C (ERCC5) ENSP00000478667.1:p.Lys1070Thr
NM_000123.3:c.3212A>C , LRG_464t1:c.3212A>C (ERCC5) NP_000114.2:p.Lys1071Thr
NM_001204425.1:c.4574A>C (BIVM-ERCC5) NP_001191354.1:p.Lys1525Thr
NM_000123.4:c.3212A>C (ERCC5) MANE Select NP_000114.3:p.Lys1071Thr
NM_001204425.2:c.4574A>C (BIVM-ERCC5) NP_001191354.2:p.Lys1525Thr