Canonical Allele Identifier: CA2115203339
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102846105T= , CM000675.2:g.102846105T= GRCh38
NC_000013.10:g.103498455T= , CM000675.1:g.103498455T= GRCh37
NC_000013.9:g.102296456T= NCBI36
NG_007146.1:g.5282T= , LRG_464:g.5282T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.80T= (ERCC5)
ENST00000682869.1:n.73T= (ERCC5)
ENST00000683246.1:n.201T= (ERCC5)
ENST00000684184.1:n.70T= (ERCC5)
ENST00000638434.1:c.363-7652T= (BIVM-ERCC5)
ENST00000639118.1:c.363-3013T= (BIVM-ERCC5)
ENST00000639132.1:c.764-6013T= (BIVM-ERCC5) ENSP00000492684.1:n.764-6013T=
ENST00000639435.1:c.1451-6013T= (BIVM-ERCC5) ENSP00000491742.1:n.1451-6013T=
ENST00000651002.1:c.-162T= (ERCC5) ENSP00000498809.1:n.-162T=
ENST00000652225.2:c.-162T= (ERCC5) MANE Select ENSP00000498881.2:n.-162T=
ENST00000652613.1:c.-659T= (ERCC5) ENSP00000498357.1:n.-659T=
ENST00000355739.8:c.-162T= (ERCC5) ENSP00000347978.4:n.-162T=
ENST00000472151.1:c.-162T= (ERCC5) ENSP00000436083.1:n.-162T=
ENST00000535557.5:c.-162T= (ERCC5) ENSP00000442117.1:n.-162T=
ENST00000602836.1:c.1365-6013T= (BIVM-ERCC5)
NM_000123.3:c.-162T= , LRG_464t1:c.-162T= (ERCC5) NP_000114.2:n.-162T=
NM_001204425.1:c.1451-6013T= (BIVM-ERCC5) NP_001191354.1:n.1451-6013T=
NM_000123.4:c.-162T= (ERCC5) MANE Select NP_000114.3:n.-162T=
NM_001204425.2:c.1451-6013T= (BIVM-ERCC5) NP_001191354.2:n.1451-6013T=