Canonical Allele Identifier: CA1933517614

Gene: GSTO2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104279427A= , CM000672.2:g.104279427A=	GRCh38
NC_000010.10:g.106039185A= , CM000672.1:g.106039185A=	GRCh37
NC_000010.9:g.106029175A=	NCBI36
NG_023363.1:g.15555A=

Transcript Alleles

HGVS	Amino-acid Change
NM_183239.2:c.424A= MANE Select	NP_899062.1:p.Asn142=
ENST00000338595.7:c.424A= MANE Select	ENSP00000345023.1:p.Asn142=
NM_001191013.1:c.366+1311A=	NP_001177942.1:n.366+1311A=
NM_001191013.2:c.366+1311A=	NP_001177942.1:n.366+1311A=
NM_001191014.1:c.340A=	NP_001177943.1:p.Asn114=
NM_001191014.2:c.340A=	NP_001177943.1:p.Asn114=
NM_001191015.1:c.282+1311A=	NP_001177944.1:n.282+1311A=
NM_001191015.2:c.282+1311A=	NP_001177944.1:n.282+1311A=
NM_183239.1:c.424A=	NP_899062.1:p.Asn142=
ENST00000338595.6:c.424A=	ENSP00000345023.1:p.Asn142=
ENST00000369707.2:c.340A=	ENSP00000358721.1:p.Asn114=
ENST00000450629.6:c.366+1311A=	ENSP00000390986.2:n.366+1311A=
ENST00000473401.5:n.275+1311A=
ENST00000477078.2:n.311A=
XM_006717624.2:c.424A=	XP_006717687.1:p.Asn142=
XM_006717624.3:c.424A=	XP_006717687.1:p.Asn142=
XM_011539270.1:c.424A=	XP_011537572.1:p.Asn142=
XM_011539270.3:c.424A=	XP_011537572.1:p.Asn142=
XM_011539271.1:c.424A=	XP_011537573.1:p.Asn142=
XM_011539271.2:c.424A=	XP_011537573.1:p.Asn142=
XM_011539272.1:c.424A=	XP_011537574.1:p.Asn142=
XM_011539272.3:c.424A=	XP_011537574.1:p.Asn142=
XM_011539273.1:c.366+1311A=	XP_011537575.1:n.366+1311A=
XM_011539273.2:c.366+1311A=	XP_011537575.1:n.366+1311A=
XM_017015670.2:c.366+1311A=	XP_016871159.1:n.366+1311A=
XM_017015671.1:c.366+1311A=	XP_016871160.1:n.366+1311A=