Canonical Allele Identifier: CA2230390994

Gene: NQO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.69723925A= , CM000678.2:g.69723925A=	GRCh38
NC_000016.9:g.69757828A= , CM000678.1:g.69757828A=	GRCh37
NC_000016.8:g.68315329A=	NCBI36
NG_011504.1:g.7706T=
NG_011504.2:g.7706T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000903.3:c.7+2508T= MANE Select	NP_000894.1:n.7+2508T=
ENST00000320623.10:c.7+2508T= MANE Select	ENSP00000319788.5:n.7+2508T=
NM_000903.2:c.7+2508T=	NP_000894.1:n.7+2508T=
NM_001025433.1:c.7+2508T=	NP_001020604.1:n.7+2508T=
NM_001025433.2:c.7+2508T=	NP_001020604.1:n.7+2508T=
NM_001025434.1:c.7+2508T=	NP_001020605.1:n.7+2508T=
NM_001025434.2:c.7+2508T=	NP_001020605.1:n.7+2508T=
NM_001286137.1:c.7+2508T=	NP_001273066.1:n.7+2508T=
NM_001286137.2:c.7+2508T=	NP_001273066.1:n.7+2508T=
ENST00000320623.9:c.7+2508T=	ENSP00000319788.5:n.7+2508T=
ENST00000379046.6:c.7+2508T=	ENSP00000368334.2:n.7+2508T=
ENST00000379047.7:c.7+2508T=	ENSP00000368335.3:n.7+2508T=
ENST00000439109.6:c.7+2508T=	ENSP00000398330.2:n.7+2508T=
ENST00000561500.5:c.7+2508T=	ENSP00000456282.1:n.7+2508T=
ENST00000564043.1:c.-57+2576T=	ENSP00000455020.1:n.-57+2576T=
ENST00000569118.1:n.93+2508T=