Canonical Allele Identifier: CA388673417
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102873260T>C , CM000675.2:g.102873260T>C GRCh38
NC_000013.10:g.103525610T>C , CM000675.1:g.103525610T>C GRCh37
NC_000013.9:g.102323611T>C NCBI36
NG_007146.1:g.32437T>C , LRG_464:g.32437T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.3982T>C (ERCC5)
ENST00000682869.1:n.3530T>C (ERCC5)
ENST00000683246.1:n.4518T>C (ERCC5)
ENST00000683642.1:n.3111T>C (ERCC5)
ENST00000639132.1:c.3556T>C (BIVM-ERCC5) ENSP00000492684.1:p.Phe1186Leu
ENST00000639435.1:c.4243T>C (BIVM-ERCC5) ENSP00000491742.1:p.Phe1415Leu
ENST00000651002.1:c.*2642T>C (ERCC5) ENSP00000498809.1:n.*2642T>C
ENST00000651055.1:n.3009-1T>C (ERCC5)
ENST00000651281.1:n.3249T>C (ERCC5)
ENST00000651387.1:n.2365T>C (ERCC5)
ENST00000651470.1:c.*53T>C (ERCC5) ENSP00000498701.1:n.*53T>C
ENST00000652225.2:c.2881T>C (ERCC5) MANE Select ENSP00000498881.2:p.Phe961Leu
ENST00000652613.1:c.2377T>C (ERCC5) ENSP00000498357.1:p.Phe793Leu
ENST00000355739.8:c.2881T>C (ERCC5) ENSP00000347978.4:p.Phe961Leu
ENST00000375954.1:c.580T>C (ERCC5) ENSP00000365121.1:p.Phe194Leu
ENST00000610537.4:c.2878T>C (ERCC5) ENSP00000478667.1:p.Phe960Leu
NM_000123.3:c.2881T>C , LRG_464t1:c.2881T>C (ERCC5) NP_000114.2:p.Phe961Leu
NM_001204425.1:c.4243T>C (BIVM-ERCC5) NP_001191354.1:p.Phe1415Leu
NM_000123.4:c.2881T>C (ERCC5) MANE Select NP_000114.3:p.Phe961Leu
NM_001204425.2:c.4243T>C (BIVM-ERCC5) NP_001191354.2:p.Phe1415Leu