Canonical Allele Identifier: CA2254005596

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27762841T= , CM000679.2:g.27762841T=	GRCh38
NC_000017.10:g.26089867T= , CM000679.1:g.26089867T=	GRCh37
NC_000017.9:g.23113994T=	NCBI36
NG_011470.1:g.42689A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000625.4:c.2757A= MANE Select	NP_000616.3:p.Thr919=
ENST00000313735.11:c.2757A= MANE Select	ENSP00000327251.6:p.Thr919=
ENST00000313735.10:c.2757A=	ENSP00000327251.6:p.Thr919=
ENST00000621962.1:c.2640A=	ENSP00000482291.1:p.Thr880=
ENST00000646938.1:c.2754A=	ENSP00000494870.1:p.Thr918=
ENST00000697337.1:c.*3421A=	ENSP00000513259.1:n.*3421A=
ENST00000697338.1:c.2605A=	ENSP00000513260.1:n.2605A=
ENST00000697339.1:c.1719A=	ENSP00000513261.1:p.Thr573=
ENST00000697340.1:c.*1470A=	ENSP00000513262.1:n.*1470A=
XM_011524859.1:c.2757A=	XP_011523161.1:p.Thr919=
XM_011524860.1:c.2754A=	XP_011523162.1:p.Thr918=
XM_011524861.1:c.2685A=	XP_011523163.1:p.Thr895=
XM_011524862.1:c.2091A=	XP_011523164.1:p.Thr697=