Canonical Allele Identifier: CA388574184
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102862900A>C , CM000675.2:g.102862900A>C GRCh38
NC_000013.10:g.103515250A>C , CM000675.1:g.103515250A>C GRCh37
NC_000013.9:g.102313251A>C NCBI36
NG_007146.1:g.22077A>C , LRG_464:g.22077A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.1992A>C (ERCC5)
ENST00000682869.1:n.2400A>C (ERCC5)
ENST00000683246.1:n.2528A>C (ERCC5)
ENST00000639132.1:c.2426A>C (BIVM-ERCC5) ENSP00000492684.1:p.Gln809Pro
ENST00000639435.1:c.3113A>C (BIVM-ERCC5) ENSP00000491742.1:p.Gln1038Pro
ENST00000651002.1:c.*1512A>C (ERCC5) ENSP00000498809.1:n.*1512A>C
ENST00000651055.1:n.1880A>C (ERCC5)
ENST00000651281.1:n.2119A>C (ERCC5)
ENST00000651387.1:n.1235A>C (ERCC5)
ENST00000651470.1:c.1751A>C (ERCC5) ENSP00000498701.1:p.Gln584Pro
ENST00000652225.2:c.1751A>C (ERCC5) MANE Select ENSP00000498881.2:p.Gln584Pro
ENST00000652613.1:c.1247A>C (ERCC5) ENSP00000498357.1:p.Gln416Pro
ENST00000355739.8:c.1751A>C (ERCC5) ENSP00000347978.4:p.Gln584Pro
ENST00000602836.1:c.3027A>C (BIVM-ERCC5)
ENST00000610537.4:c.1751A>C (ERCC5) ENSP00000478667.1:p.Gln584Pro
NM_000123.3:c.1751A>C , LRG_464t1:c.1751A>C (ERCC5) NP_000114.2:p.Gln584Pro
NM_001204425.1:c.3113A>C (BIVM-ERCC5) NP_001191354.1:p.Gln1038Pro
NM_000123.4:c.1751A>C (ERCC5) MANE Select NP_000114.3:p.Gln584Pro
NM_001204425.2:c.3113A>C (BIVM-ERCC5) NP_001191354.2:p.Gln1038Pro