Canonical Allele Identifier: CA2115215380
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102873395T= , CM000675.2:g.102873395T= GRCh38
NC_000013.10:g.103525745T= , CM000675.1:g.103525745T= GRCh37
NC_000013.9:g.102323746T= NCBI36
NG_007146.1:g.32572T= , LRG_464:g.32572T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4065+52T= (ERCC5)
ENST00000682869.1:n.3613+52T= (ERCC5)
ENST00000683246.1:n.4601+52T= (ERCC5)
ENST00000683642.1:n.3194+52T= (ERCC5)
ENST00000639132.1:c.3639+52T= (BIVM-ERCC5) ENSP00000492684.1:n.3639+52T=
ENST00000639435.1:c.4326+52T= (BIVM-ERCC5) ENSP00000491742.1:n.4326+52T=
ENST00000651002.1:c.*2725+52T= (ERCC5) ENSP00000498809.1:n.*2725+52T=
ENST00000651055.1:n.3091+52T= (ERCC5)
ENST00000651281.1:n.3332+52T= (ERCC5)
ENST00000651387.1:n.2448+52T= (ERCC5)
ENST00000651470.1:c.*136+52T= (ERCC5) ENSP00000498701.1:n.*136+52T=
ENST00000652225.2:c.2964+52T= (ERCC5) MANE Select ENSP00000498881.2:n.2964+52T=
ENST00000652613.1:c.2460+52T= (ERCC5) ENSP00000498357.1:n.2460+52T=
ENST00000355739.8:c.2964+52T= (ERCC5) ENSP00000347978.4:n.2964+52T=
ENST00000375954.1:c.663+52T= (ERCC5) ENSP00000365121.1:n.663+52T=
ENST00000610537.4:c.2961+52T= (ERCC5) ENSP00000478667.1:n.2961+52T=
NM_000123.3:c.2964+52T= , LRG_464t1:c.2964+52T= (ERCC5) NP_000114.2:n.2964+52T=
NM_001204425.1:c.4326+52T= (BIVM-ERCC5) NP_001191354.1:n.4326+52T=
NM_000123.4:c.2964+52T= (ERCC5) MANE Select NP_000114.3:n.2964+52T=
NM_001204425.2:c.4326+52T= (BIVM-ERCC5) NP_001191354.2:n.4326+52T=