Canonical Allele Identifier: CA2254008438

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769573T= , CM000679.2:g.27769573T=	GRCh38
NC_000017.10:g.26096599T= , CM000679.1:g.26096599T=	GRCh37
NC_000017.9:g.23120726T=	NCBI36
NG_011470.1:g.35957A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2557A=	ENSP00000513259.1:n.*2557A=
ENST00000697338.1:c.1669A=	ENSP00000513260.1:n.1669A=
ENST00000697339.1:c.855A=	ENSP00000513261.1:p.Lys285=
ENST00000697340.1:c.*538A=	ENSP00000513262.1:n.*538A=
ENST00000697341.1:n.1791A=
ENST00000313735.11:c.1821A= MANE Select	ENSP00000327251.6:p.Lys607=
ENST00000646938.1:c.1818A=	ENSP00000494870.1:p.Lys606=
ENST00000313735.10:c.1821A=	ENSP00000327251.6:p.Lys607=
ENST00000621962.1:c.1704A=	ENSP00000482291.1:p.Lys568=
NM_000625.4:c.1821A= MANE Select	NP_000616.3:p.Lys607=
XM_011524859.1:c.1821A=	XP_011523161.1:p.Lys607=
XM_011524860.1:c.1818A=	XP_011523162.1:p.Lys606=
XM_011524861.1:c.1821A=	XP_011523163.1:p.Lys607=
XM_011524862.1:c.1155A=	XP_011523164.1:p.Lys385=