Canonical Allele Identifier: CA2115216515
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875654T= , CM000675.2:g.102875654T= GRCh38
NC_000013.10:g.103528004T= , CM000675.1:g.103528004T= GRCh37
NC_000013.9:g.102326005T= NCBI36
NG_007146.1:g.34831T= , LRG_464:g.34831T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682632.1:n.4413T= (ERCC5)
ENST00000682869.1:n.3961T= (ERCC5)
ENST00000683246.1:n.4949T= (ERCC5)
ENST00000683642.1:n.3542T= (ERCC5)
ENST00000639132.1:c.3987T= (BIVM-ERCC5) ENSP00000492684.1:p.Asp1329=
ENST00000639435.1:c.4674T= (BIVM-ERCC5) ENSP00000491742.1:p.Asp1558=
ENST00000651002.1:c.*3073T= (ERCC5) ENSP00000498809.1:n.*3073T=
ENST00000651055.1:n.3439T= (ERCC5)
ENST00000651281.1:n.3680T= (ERCC5)
ENST00000651387.1:n.2796T= (ERCC5)
ENST00000651470.1:c.*484T= (ERCC5) ENSP00000498701.1:n.*484T=
ENST00000652225.2:c.3312T= (ERCC5) MANE Select ENSP00000498881.2:p.Asp1104=
ENST00000652613.1:c.2808T= (ERCC5) ENSP00000498357.1:p.Asp936=
ENST00000355739.8:c.3312T= (ERCC5) ENSP00000347978.4:p.Asp1104=
ENST00000375954.1:c.1011T= (ERCC5) ENSP00000365121.1:p.Asp337=
ENST00000472247.1:n.472T= (ERCC5)
ENST00000610537.4:c.3309T= (ERCC5) ENSP00000478667.1:p.Asp1103=
NM_000123.3:c.3312T= , LRG_464t1:c.3312T= (ERCC5) NP_000114.2:p.Asp1104=
NM_001204425.1:c.4674T= (BIVM-ERCC5) NP_001191354.1:p.Asp1558=
NM_000123.4:c.3312T= (ERCC5) MANE Select NP_000114.3:p.Asp1104=
NM_001204425.2:c.4674T= (BIVM-ERCC5) NP_001191354.2:p.Asp1558=