Canonical Allele Identifier: CA2115216471
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875569C= , CM000675.2:g.102875569C= GRCh38
NC_000013.10:g.103527919C= , CM000675.1:g.103527919C= GRCh37
NC_000013.9:g.102325920C= NCBI36
NG_007146.1:g.34746C= , LRG_464:g.34746C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4328C= (ERCC5)
ENST00000682869.1:n.3876C= (ERCC5)
ENST00000683246.1:n.4864C= (ERCC5)
ENST00000683642.1:n.3457C= (ERCC5)
ENST00000639132.1:c.3902C= (BIVM-ERCC5) ENSP00000492684.1:p.Ser1301=
ENST00000639435.1:c.4589C= (BIVM-ERCC5) ENSP00000491742.1:p.Ser1530=
ENST00000651002.1:c.*2988C= (ERCC5) ENSP00000498809.1:n.*2988C=
ENST00000651055.1:n.3354C= (ERCC5)
ENST00000651281.1:n.3595C= (ERCC5)
ENST00000651387.1:n.2711C= (ERCC5)
ENST00000651470.1:c.*399C= (ERCC5) ENSP00000498701.1:n.*399C=
ENST00000652225.2:c.3227C= (ERCC5) MANE Select ENSP00000498881.2:p.Ser1076=
ENST00000652613.1:c.2723C= (ERCC5) ENSP00000498357.1:p.Ser908=
ENST00000355739.8:c.3227C= (ERCC5) ENSP00000347978.4:p.Ser1076=
ENST00000375954.1:c.926C= (ERCC5) ENSP00000365121.1:p.Ser309=
ENST00000472247.1:n.387C= (ERCC5)
ENST00000610537.4:c.3224C= (ERCC5) ENSP00000478667.1:p.Ser1075=
NM_000123.3:c.3227C= , LRG_464t1:c.3227C= (ERCC5) NP_000114.2:p.Ser1076=
NM_001204425.1:c.4589C= (BIVM-ERCC5) NP_001191354.1:p.Ser1530=
NM_000123.4:c.3227C= (ERCC5) MANE Select NP_000114.3:p.Ser1076=
NM_001204425.2:c.4589C= (BIVM-ERCC5) NP_001191354.2:p.Ser1530=