Canonical Allele Identifier: CA2254008393

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769537G= , CM000679.2:g.27769537G=	GRCh38
NC_000017.10:g.26096563G= , CM000679.1:g.26096563G=	GRCh37
NC_000017.9:g.23120690G=	NCBI36
NG_011470.1:g.35993C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2593C=	ENSP00000513259.1:n.*2593C=
ENST00000697338.1:c.1705C=	ENSP00000513260.1:n.1705C=
ENST00000697339.1:c.891C=	ENSP00000513261.1:p.Phe297=
ENST00000697340.1:c.*574C=	ENSP00000513262.1:n.*574C=
ENST00000697341.1:n.1827C=
ENST00000313735.11:c.1857C= MANE Select	ENSP00000327251.6:p.Phe619=
ENST00000646938.1:c.1854C=	ENSP00000494870.1:p.Phe618=
ENST00000313735.10:c.1857C=	ENSP00000327251.6:p.Phe619=
ENST00000621962.1:c.1740C=	ENSP00000482291.1:p.Phe580=
NM_000625.4:c.1857C= MANE Select	NP_000616.3:p.Phe619=
XM_011524859.1:c.1857C=	XP_011523161.1:p.Phe619=
XM_011524860.1:c.1854C=	XP_011523162.1:p.Phe618=
XM_011524861.1:c.1857C=	XP_011523163.1:p.Phe619=
XM_011524862.1:c.1191C=	XP_011523164.1:p.Phe397=