Canonical Allele Identifier: CA376726647
Gene: ERCC6 HGNC NCBI

Linked Data

dbSNP Id: rs1315875811

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49493238C>A , CM000672.2:g.49493238C>A GRCh38
NC_000010.10:g.50701284C>A , CM000672.1:g.50701284C>A GRCh37
NC_000010.9:g.50371290C>A NCBI36
NG_009442.1:g.50864G>T , LRG_465:g.50864G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355832.10:c.1700G>T MANE Select ENSP00000348089.5:p.Gly567Val
ENST00000681632.1:n.1778G>T
ENST00000681659.1:c.1541G>T ENSP00000505631.1:p.Gly514Val
ENST00000355832.9:c.1700G>T ENSP00000348089.5:p.Gly567Val
ENST00000475116.1:n.275+7300G>T
ENST00000623073.3:c.101G>T ENSP00000485650.1:p.Gly34Val
ENST00000623115.3:c.-70+7300G>T ENSP00000485321.1:n.-70+7300G>T
ENST00000623318.1:c.101G>T ENSP00000485423.1:p.Gly34Val
NM_000124.3:c.1700G>T NP_000115.1:p.Gly567Val
NM_001346440.1:c.1700G>T NP_001333369.1:p.Gly567Val
NM_000124.4:c.1700G>T MANE Select NP_000115.1:p.Gly567Val
NM_001346440.2:c.1700G>T NP_001333369.1:p.Gly567Val