Canonical Allele Identifier: CA376726478

Gene: ERCC6

Linked Data

• ClinVar Variation Id: 984139
• ClinVar RCV Id: RCV001264147
• dbSNP Id: rs768188064
• MyVariant Identifiers: chr10:g.50701207T>A (hg19) ; chr10:g.49493161T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49493161T>A , CM000672.2:g.49493161T>A	GRCh38
NC_000010.10:g.50701207T>A , CM000672.1:g.50701207T>A	GRCh37
NC_000010.9:g.50371213T>A	NCBI36
NG_009442.1:g.50941A>T , LRG_465:g.50941A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.1777A>T MANE Select	ENSP00000348089.5:p.Arg593Ter
ENST00000681632.1:n.1855A>T
ENST00000681659.1:c.1618A>T	ENSP00000505631.1:p.Arg540Ter
ENST00000355832.9:c.1777A>T	ENSP00000348089.5:p.Arg593Ter
ENST00000475116.1:n.275+7377A>T
ENST00000623073.3:c.178A>T	ENSP00000485650.1:p.Arg60Ter
ENST00000623115.3:c.-70+7377A>T	ENSP00000485321.1:n.-70+7377A>T
ENST00000623318.1:c.178A>T	ENSP00000485423.1:p.Arg60Ter
NM_000124.3:c.1777A>T	NP_000115.1:p.Arg593Ter
NM_001346440.1:c.1777A>T	NP_001333369.1:p.Arg593Ter
NM_000124.4:c.1777A>T MANE Select	NP_000115.1:p.Arg593Ter
NM_001346440.2:c.1777A>T	NP_001333369.1:p.Arg593Ter