Canonical Allele Identifier: CA2254014164

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27782091T= , CM000679.2:g.27782091T=	GRCh38
NC_000017.10:g.26109117T= , CM000679.1:g.26109117T=	GRCh37
NC_000017.9:g.23133244T=	NCBI36
NG_011470.1:g.23439A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*92A=	ENSP00000513259.1:n.*92A=
ENST00000697338.1:c.494A=	ENSP00000513260.1:n.494A=
ENST00000697339.1:c.315+6718A=	ENSP00000513261.1:n.315+6718A=
ENST00000697340.1:c.643A=	ENSP00000513262.1:p.Ser215=
ENST00000697341.1:n.616A=
ENST00000313735.11:c.646A= MANE Select	ENSP00000327251.6:p.Ser216=
ENST00000646938.1:c.643A=	ENSP00000494870.1:p.Ser215=
ENST00000313735.10:c.646A=	ENSP00000327251.6:p.Ser216=
ENST00000621962.1:c.646A=	ENSP00000482291.1:p.Ser216=
NM_000625.4:c.646A= MANE Select	NP_000616.3:p.Ser216=
XM_011524859.1:c.646A=	XP_011523161.1:p.Ser216=
XM_011524860.1:c.643A=	XP_011523162.1:p.Ser215=
XM_011524861.1:c.646A=	XP_011523163.1:p.Ser216=
XM_011524862.1:c.-21A=	XP_011523164.1:n.-21A=