Canonical Allele Identifier: CA2254008413

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769563T= , CM000679.2:g.27769563T=	GRCh38
NC_000017.10:g.26096589T= , CM000679.1:g.26096589T=	GRCh37
NC_000017.9:g.23120716T=	NCBI36
NG_011470.1:g.35967A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2567A=	ENSP00000513259.1:n.*2567A=
ENST00000697338.1:c.1679A=	ENSP00000513260.1:n.1679A=
ENST00000697339.1:c.865A=	ENSP00000513261.1:p.Met289=
ENST00000697340.1:c.*548A=	ENSP00000513262.1:n.*548A=
ENST00000697341.1:n.1801A=
ENST00000313735.11:c.1831A= MANE Select	ENSP00000327251.6:p.Met611=
ENST00000646938.1:c.1828A=	ENSP00000494870.1:p.Met610=
ENST00000313735.10:c.1831A=	ENSP00000327251.6:p.Met611=
ENST00000621962.1:c.1714A=	ENSP00000482291.1:p.Met572=
NM_000625.4:c.1831A= MANE Select	NP_000616.3:p.Met611=
XM_011524859.1:c.1831A=	XP_011523161.1:p.Met611=
XM_011524860.1:c.1828A=	XP_011523162.1:p.Met610=
XM_011524861.1:c.1831A=	XP_011523163.1:p.Met611=
XM_011524862.1:c.1165A=	XP_011523164.1:p.Met389=