Canonical Allele Identifier: CA1908772578

Gene: ERCC6

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.1777A= MANE Select	ENSP00000348089.5:p.Arg593=
ENST00000681632.1:n.1855A=
ENST00000681659.1:c.1618A=	ENSP00000505631.1:p.Arg540=
ENST00000355832.9:c.1777A=	ENSP00000348089.5:p.Arg593=
ENST00000475116.1:n.275+7377A=
ENST00000623073.3:c.178A=	ENSP00000485650.1:p.Arg60=
ENST00000623115.3:c.-70+7377A=	ENSP00000485321.1:n.-70+7377A=
ENST00000623318.1:c.178A=	ENSP00000485423.1:p.Arg60=
NM_000124.3:c.1777A=	NP_000115.1:p.Arg593=
NM_001346440.1:c.1777A=	NP_001333369.1:p.Arg593=
NM_000124.4:c.1777A= MANE Select	NP_000115.1:p.Arg593=
NM_001346440.2:c.1777A=	NP_001333369.1:p.Arg593=