Canonical Allele Identifier: CA2809097934

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27782241_27782242del , CM000679.2:g.27782241_27782242del	GRCh38
NC_000017.10:g.26109267_26109268del , CM000679.1:g.26109267_26109268del	GRCh37
NC_000017.9:g.23133394_23133395del	NCBI36
NG_011470.1:g.23289_23290del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*77-135_*77-134del	ENSP00000513259.1:n.*77-135_*77-134del
ENST00000697338.1:c.479-135_479-134del	ENSP00000513260.1:n.479-135_479-134del
ENST00000697339.1:c.315+6568_315+6569del	ENSP00000513261.1:n.315+6568_315+6569del
ENST00000697340.1:c.628-135_628-134del	ENSP00000513262.1:n.628-135_628-134del
ENST00000697341.1:n.601-135_601-134del
ENST00000313735.11:c.631-135_631-134del MANE Select	ENSP00000327251.6:n.631-135_631-134del
ENST00000646938.1:c.628-135_628-134del	ENSP00000494870.1:n.628-135_628-134del
ENST00000313735.10:c.631-135_631-134del	ENSP00000327251.6:n.631-135_631-134del
ENST00000621962.1:c.631-135_631-134del	ENSP00000482291.1:n.631-135_631-134del
NM_000625.4:c.631-135_631-134del MANE Select	NP_000616.3:n.631-135_631-134del
XM_011524859.1:c.631-135_631-134del	XP_011523161.1:n.631-135_631-134del
XM_011524860.1:c.628-135_628-134del	XP_011523162.1:n.628-135_628-134del
XM_011524861.1:c.631-135_631-134del	XP_011523163.1:n.631-135_631-134del
XM_011524862.1:c.-36-135_-36-134del	XP_011523164.1:n.-36-135_-36-134del