Canonical Allele Identifier: CA1606482381

Gene: NQO2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.3000069A= , CM000668.2:g.3000069A=	GRCh38
NC_000006.11:g.3000303A= , CM000668.1:g.3000303A=	GRCh37
NC_000006.10:g.2945302A=	NCBI36
NG_034013.1:g.5254A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338130.7:c.-617A=	ENSP00000337773.2:n.-617A=
ENST00000380455.11:c.-102A= MANE Select	ENSP00000369822.4:n.-102A=
ENST00000397717.7:c.-223A=	ENSP00000380829.2:n.-223A=
ENST00000338130.6:c.-617A=	ENSP00000337773.2:n.-617A=
ENST00000380441.5:c.-259A=	ENSP00000369806.1:n.-259A=
ENST00000380454.8:c.-102A=	ENSP00000369821.4:n.-102A=
ENST00000380455.8:c.-102A=	ENSP00000369822.4:n.-102A=
ENST00000380472.7:c.-86+6016A=	ENSP00000369839.3:n.-86+6016A=
ENST00000397717.6:c.-223A=	ENSP00000380829.2:n.-223A=
ENST00000426637.5:c.-86+6016A=	ENSP00000406951.1:n.-86+6016A=
NM_000904.4:c.-102A=	NP_000895.2:n.-102A=
NM_001290221.1:c.-617A=	NP_001277150.1:n.-617A=
NM_001290222.1:c.-102A=	NP_001277151.1:n.-102A=
XM_005249148.2:c.-259A=	XP_005249205.1:n.-259A=
XM_005249149.2:c.-380A=	XP_005249206.1:n.-380A=
XM_005249150.2:c.-223A=	XP_005249207.1:n.-223A=
XM_006715100.1:c.-460A=	XP_006715163.1:n.-460A=
XM_011514643.1:c.-600-1981A=	XP_011512945.1:n.-600-1981A=
XM_011514644.1:c.-86+6016A=	XP_011512946.1:n.-86+6016A=
XM_011514646.1:c.-86+1025A=	XP_011512948.1:n.-86+1025A=
NM_000904.6:c.-102A= MANE Select	NP_000895.2:n.-102A=
NM_001290221.2:c.-617A=	NP_001277150.1:n.-617A=
NM_001290222.2:c.-102A=	NP_001277151.1:n.-102A=
NM_001318940.2:c.-384A=	NP_001305869.1:n.-384A=