Canonical Allele Identifier: CA2254006776

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27765537C= , CM000679.2:g.27765537C=	GRCh38
NC_000017.10:g.26092563C= , CM000679.1:g.26092563C=	GRCh37
NC_000017.9:g.23116690C=	NCBI36
NG_011470.1:g.39993G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*3092+70G=	ENSP00000513259.1:n.*3092+70G=
ENST00000697338.1:c.2274G=	ENSP00000513260.1:n.2274G=
ENST00000697339.1:c.1390+70G=	ENSP00000513261.1:n.1390+70G=
ENST00000697340.1:c.*1143G=	ENSP00000513262.1:n.*1143G=
ENST00000697341.1:n.2396G=
ENST00000313735.11:c.2426G= MANE Select	ENSP00000327251.6:p.Ser809=
ENST00000646938.1:c.2423G=	ENSP00000494870.1:p.Ser808=
ENST00000313735.10:c.2426G=	ENSP00000327251.6:p.Ser809=
ENST00000621962.1:c.2309G=	ENSP00000482291.1:p.Ser770=
NM_000625.4:c.2426G= MANE Select	NP_000616.3:p.Ser809=
XM_011524859.1:c.2426G=	XP_011523161.1:p.Ser809=
XM_011524860.1:c.2423G=	XP_011523162.1:p.Ser808=
XM_011524861.1:c.2356+70G=	XP_011523163.1:n.2356+70G=
XM_011524862.1:c.1760G=	XP_011523164.1:p.Ser587=