Canonical Allele Identifier: CA2254008420

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769568A= , CM000679.2:g.27769568A=	GRCh38
NC_000017.10:g.26096594A= , CM000679.1:g.26096594A=	GRCh37
NC_000017.9:g.23120721A=	NCBI36
NG_011470.1:g.35962T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2562T=	ENSP00000513259.1:n.*2562T=
ENST00000697338.1:c.1674T=	ENSP00000513260.1:n.1674T=
ENST00000697339.1:c.860T=	ENSP00000513261.1:p.Leu287=
ENST00000697340.1:c.*543T=	ENSP00000513262.1:n.*543T=
ENST00000697341.1:n.1796T=
ENST00000313735.11:c.1826T= MANE Select	ENSP00000327251.6:p.Leu609=
ENST00000646938.1:c.1823T=	ENSP00000494870.1:p.Leu608=
ENST00000313735.10:c.1826T=	ENSP00000327251.6:p.Leu609=
ENST00000621962.1:c.1709T=	ENSP00000482291.1:p.Leu570=
NM_000625.4:c.1826T= MANE Select	NP_000616.3:p.Leu609=
XM_011524859.1:c.1826T=	XP_011523161.1:p.Leu609=
XM_011524860.1:c.1823T=	XP_011523162.1:p.Leu608=
XM_011524861.1:c.1826T=	XP_011523163.1:p.Leu609=
XM_011524862.1:c.1160T=	XP_011523164.1:p.Leu387=