Canonical Allele Identifier: CA727715899

Gene: NOS2

Linked Data

• dbSNP Id: rs1328724363
• MyVariant Identifiers: chr17:g.26109292_26109293del (hg19) ; chr17:g.27782266_27782267del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27782267_27782268del , CM000679.2:g.27782267_27782268del	GRCh38
NC_000017.10:g.26109293_26109294del , CM000679.1:g.26109293_26109294del	GRCh37
NC_000017.9:g.23133420_23133421del	NCBI36
NG_011470.1:g.23263_23264del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*77-161_*77-160del	ENSP00000513259.1:n.*77-161_*77-160del
ENST00000697338.1:c.479-161_479-160del	ENSP00000513260.1:n.479-161_479-160del
ENST00000697339.1:c.315+6542_315+6543del	ENSP00000513261.1:n.315+6542_315+6543del
ENST00000697340.1:c.628-161_628-160del	ENSP00000513262.1:n.628-161_628-160del
ENST00000697341.1:n.601-161_601-160del
ENST00000313735.11:c.631-161_631-160del MANE Select	ENSP00000327251.6:n.631-161_631-160del
ENST00000646938.1:c.628-161_628-160del	ENSP00000494870.1:n.628-161_628-160del
ENST00000313735.10:c.631-161_631-160del	ENSP00000327251.6:n.631-161_631-160del
ENST00000621962.1:c.631-161_631-160del	ENSP00000482291.1:n.631-161_631-160del
NM_000625.4:c.631-161_631-160del MANE Select	NP_000616.3:n.631-161_631-160del
XM_011524859.1:c.631-161_631-160del	XP_011523161.1:n.631-161_631-160del
XM_011524860.1:c.628-161_628-160del	XP_011523162.1:n.628-161_628-160del
XM_011524861.1:c.631-161_631-160del	XP_011523163.1:n.631-161_631-160del
XM_011524862.1:c.-36-161_-36-160del	XP_011523164.1:n.-36-161_-36-160del