Canonical Allele Identifier: CA398301442

Gene: NOS2

Linked Data

• MyVariant Identifiers: chr17:g.26096578C>A (hg19) ; chr17:g.27769552C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769552C>A , CM000679.2:g.27769552C>A	GRCh38
NC_000017.10:g.26096578C>A , CM000679.1:g.26096578C>A	GRCh37
NC_000017.9:g.23120705C>A	NCBI36
NG_011470.1:g.35978G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2578G>T	ENSP00000513259.1:n.*2578G>T
ENST00000697338.1:c.1690G>T	ENSP00000513260.1:n.1690G>T
ENST00000697339.1:c.876G>T	ENSP00000513261.1:p.Glu292Asp
ENST00000697340.1:c.*559G>T	ENSP00000513262.1:n.*559G>T
ENST00000697341.1:n.1812G>T
ENST00000313735.11:c.1842G>T MANE Select	ENSP00000327251.6:p.Glu614Asp
ENST00000646938.1:c.1839G>T	ENSP00000494870.1:p.Glu613Asp
ENST00000313735.10:c.1842G>T	ENSP00000327251.6:p.Glu614Asp
ENST00000621962.1:c.1725G>T	ENSP00000482291.1:p.Glu575Asp
NM_000625.4:c.1842G>T MANE Select	NP_000616.3:p.Glu614Asp
XM_011524859.1:c.1842G>T	XP_011523161.1:p.Glu614Asp
XM_011524860.1:c.1839G>T	XP_011523162.1:p.Glu613Asp
XM_011524861.1:c.1842G>T	XP_011523163.1:p.Glu614Asp
XM_011524862.1:c.1176G>T	XP_011523164.1:p.Glu392Asp