Canonical Allele Identifier: CA2230368376

Gene: NQO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.69711242G= , CM000678.2:g.69711242G=	GRCh38
NC_000016.9:g.69745145G= , CM000678.1:g.69745145G=	GRCh37
NC_000016.8:g.68302646G=	NCBI36
NG_011504.1:g.20389C=
NG_011504.2:g.20389C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000903.3:c.559C= MANE Select	NP_000894.1:p.Pro187=
ENST00000320623.10:c.559C= MANE Select	ENSP00000319788.5:p.Pro187=
NM_000903.2:c.559C=	NP_000894.1:p.Pro187=
NM_001025433.1:c.457C=	NP_001020604.1:p.Pro153=
NM_001025433.2:c.457C=	NP_001020604.1:p.Pro153=
NM_001025434.1:c.445C=	NP_001020605.1:p.Pro149=
NM_001025434.2:c.445C=	NP_001020605.1:p.Pro149=
NM_001286137.1:c.343C=	NP_001273066.1:p.Pro115=
NM_001286137.2:c.343C=	NP_001273066.1:p.Pro115=
ENST00000320623.9:c.559C=	ENSP00000319788.5:p.Pro187=
ENST00000379046.6:c.445C=	ENSP00000368334.2:p.Pro149=
ENST00000379047.7:c.457C=	ENSP00000368335.3:p.Pro153=
ENST00000439109.6:c.343C=	ENSP00000398330.2:p.Pro115=
ENST00000561500.5:c.445C=	ENSP00000456282.1:p.Pro149=
ENST00000564043.1:c.496C=	ENSP00000455020.1:p.Pro166=