Canonical Allele Identifier: CA2254008408

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769553T= , CM000679.2:g.27769553T=	GRCh38
NC_000017.10:g.26096579T= , CM000679.1:g.26096579T=	GRCh37
NC_000017.9:g.23120706T=	NCBI36
NG_011470.1:g.35977A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2577A=	ENSP00000513259.1:n.*2577A=
ENST00000697338.1:c.1689A=	ENSP00000513260.1:n.1689A=
ENST00000697339.1:c.875A=	ENSP00000513261.1:p.Glu292=
ENST00000697340.1:c.*558A=	ENSP00000513262.1:n.*558A=
ENST00000697341.1:n.1811A=
ENST00000313735.11:c.1841A= MANE Select	ENSP00000327251.6:p.Glu614=
ENST00000646938.1:c.1838A=	ENSP00000494870.1:p.Glu613=
ENST00000313735.10:c.1841A=	ENSP00000327251.6:p.Glu614=
ENST00000621962.1:c.1724A=	ENSP00000482291.1:p.Glu575=
NM_000625.4:c.1841A= MANE Select	NP_000616.3:p.Glu614=
XM_011524859.1:c.1841A=	XP_011523161.1:p.Glu614=
XM_011524860.1:c.1838A=	XP_011523162.1:p.Glu613=
XM_011524861.1:c.1841A=	XP_011523163.1:p.Glu614=
XM_011524862.1:c.1175A=	XP_011523164.1:p.Glu392=