Canonical Allele Identifier: CA2636789689

Gene: NOS2

Linked Data

• gnomAD v4: 17-27782198-C-CCGAAACA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27782200_27782206dup , CM000679.2:g.27782200_27782206dup	GRCh38
NC_000017.10:g.26109226_26109232dup , CM000679.1:g.26109226_26109232dup	GRCh37
NC_000017.9:g.23133353_23133359dup	NCBI36
NG_011470.1:g.23325_23331dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*77-99_*77-93dup	ENSP00000513259.1:n.*77-99_*77-93dup
ENST00000697338.1:c.479-99_479-93dup	ENSP00000513260.1:n.479-99_479-93dup
ENST00000697339.1:c.315+6604_315+6610dup	ENSP00000513261.1:n.315+6604_315+6610dup
ENST00000697340.1:c.628-99_628-93dup	ENSP00000513262.1:n.628-99_628-93dup
ENST00000697341.1:n.601-99_601-93dup
ENST00000313735.11:c.631-99_631-93dup MANE Select	ENSP00000327251.6:n.631-99_631-93dup
ENST00000646938.1:c.628-99_628-93dup	ENSP00000494870.1:n.628-99_628-93dup
ENST00000313735.10:c.631-99_631-93dup	ENSP00000327251.6:n.631-99_631-93dup
ENST00000621962.1:c.631-99_631-93dup	ENSP00000482291.1:n.631-99_631-93dup
NM_000625.4:c.631-99_631-93dup MANE Select	NP_000616.3:n.631-99_631-93dup
XM_011524859.1:c.631-99_631-93dup	XP_011523161.1:n.631-99_631-93dup
XM_011524860.1:c.628-99_628-93dup	XP_011523162.1:n.628-99_628-93dup
XM_011524861.1:c.631-99_631-93dup	XP_011523163.1:n.631-99_631-93dup
XM_011524862.1:c.-36-99_-36-93dup	XP_011523164.1:n.-36-99_-36-93dup