Canonical Allele Identifier: CA2115215337
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102873290A= , CM000675.2:g.102873290A= GRCh38
NC_000013.10:g.103525640A= , CM000675.1:g.103525640A= GRCh37
NC_000013.9:g.102323641A= NCBI36
NG_007146.1:g.32467A= , LRG_464:g.32467A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682632.1:n.4012A= (ERCC5)
ENST00000682869.1:n.3560A= (ERCC5)
ENST00000683246.1:n.4548A= (ERCC5)
ENST00000683642.1:n.3141A= (ERCC5)
ENST00000639132.1:c.3586A= (BIVM-ERCC5) ENSP00000492684.1:p.Thr1196=
ENST00000639435.1:c.4273A= (BIVM-ERCC5) ENSP00000491742.1:p.Thr1425=
ENST00000651002.1:c.*2672A= (ERCC5) ENSP00000498809.1:n.*2672A=
ENST00000651055.1:n.3038A= (ERCC5)
ENST00000651281.1:n.3279A= (ERCC5)
ENST00000651387.1:n.2395A= (ERCC5)
ENST00000651470.1:c.*83A= (ERCC5) ENSP00000498701.1:n.*83A=
ENST00000652225.2:c.2911A= (ERCC5) MANE Select ENSP00000498881.2:p.Thr971=
ENST00000652613.1:c.2407A= (ERCC5) ENSP00000498357.1:p.Thr803=
ENST00000355739.8:c.2911A= (ERCC5) ENSP00000347978.4:p.Thr971=
ENST00000375954.1:c.610A= (ERCC5) ENSP00000365121.1:p.Thr204=
ENST00000610537.4:c.2908A= (ERCC5) ENSP00000478667.1:p.Thr970=
NM_000123.3:c.2911A= , LRG_464t1:c.2911A= (ERCC5) NP_000114.2:p.Thr971=
NM_001204425.1:c.4273A= (BIVM-ERCC5) NP_001191354.1:p.Thr1425=
NM_000123.4:c.2911A= (ERCC5) MANE Select NP_000114.3:p.Thr971=
NM_001204425.2:c.4273A= (BIVM-ERCC5) NP_001191354.2:p.Thr1425=