Canonical Allele Identifier: CA484968435
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.103515188T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102862838T>C , CM000675.2:g.102862838T>C GRCh38
NC_000013.10:g.103515188T>C , CM000675.1:g.103515188T>C GRCh37
NC_000013.9:g.102313189T>C NCBI36
NG_007146.1:g.22015T>C , LRG_464:g.22015T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.1930T>C (ERCC5)
ENST00000682869.1:n.2338T>C (ERCC5)
ENST00000683246.1:n.2466T>C (ERCC5)
ENST00000639132.1:c.2364T>C (BIVM-ERCC5) ENSP00000492684.1:p.Ser788=
ENST00000639435.1:c.3051T>C (BIVM-ERCC5) ENSP00000491742.1:p.Ser1017=
ENST00000651002.1:c.*1450T>C (ERCC5) ENSP00000498809.1:n.*1450T>C
ENST00000651055.1:n.1818T>C (ERCC5)
ENST00000651281.1:n.2057T>C (ERCC5)
ENST00000651387.1:n.1173T>C (ERCC5)
ENST00000651470.1:c.1689T>C (ERCC5) ENSP00000498701.1:p.Ser563=
ENST00000652225.2:c.1689T>C (ERCC5) MANE Select ENSP00000498881.2:p.Ser563=
ENST00000652613.1:c.1185T>C (ERCC5) ENSP00000498357.1:p.Ser395=
ENST00000355739.8:c.1689T>C (ERCC5) ENSP00000347978.4:p.Ser563=
ENST00000602836.1:c.2965T>C (BIVM-ERCC5)
ENST00000610537.4:c.1689T>C (ERCC5) ENSP00000478667.1:p.Ser563=
NM_000123.3:c.1689T>C , LRG_464t1:c.1689T>C (ERCC5) NP_000114.2:p.Ser563=
NM_001204425.1:c.3051T>C (BIVM-ERCC5) NP_001191354.1:p.Ser1017=
NM_000123.4:c.1689T>C (ERCC5) MANE Select NP_000114.3:p.Ser563=
NM_001204425.2:c.3051T>C (BIVM-ERCC5) NP_001191354.2:p.Ser1017=