Canonical Allele Identifier: CA2254014867

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27783801_27783802delinsAG , CM000679.2:g.27783801_27783802delinsAG	GRCh38
NC_000017.10:g.26110827_26110828delinsAG , CM000679.1:g.26110827_26110828delinsAG	GRCh37
NC_000017.9:g.23134954_23134955delinsAG	NCBI36
NG_011470.1:g.21728_21729delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000697337.1:c.319-696_319-695delinsCT	ENSP00000513259.1:n.319-696_319-695delins...
ENST00000697338.1:c.316-696_316-695delinsCT	ENSP00000513260.1:n.316-696_316-695delins...
ENST00000697339.1:c.315+5007_315+5008delinsCT	ENSP00000513261.1:n.315+5007_315+5008deli...
ENST00000697340.1:c.465-696_465-695delinsCT	ENSP00000513262.1:n.465-696_465-695delins...
ENST00000697341.1:n.438-696_438-695delinsCT
ENST00000313735.11:c.468-696_468-695delinsCT MANE Select	ENSP00000327251.6:n.468-696_468-695delins...
ENST00000646938.1:c.465-696_465-695delinsCT	ENSP00000494870.1:n.465-696_465-695delins...
ENST00000313735.10:c.468-696_468-695delinsCT	ENSP00000327251.6:n.468-696_468-695delins...
ENST00000621962.1:c.468-696_468-695delinsCT	ENSP00000482291.1:n.468-696_468-695delins...
NM_000625.4:c.468-696_468-695delinsCT MANE Select	NP_000616.3:n.468-696_468-695delinsCT
XM_011524859.1:c.468-696_468-695delinsCT	XP_011523161.1:n.468-696_468-695delinsCT
XM_011524860.1:c.465-696_465-695delinsCT	XP_011523162.1:n.465-696_465-695delinsCT
XM_011524861.1:c.468-696_468-695delinsCT	XP_011523163.1:n.468-696_468-695delinsCT
XM_011524862.1:c.-199-696_-199-695delinsCT	XP_011523164.1:n.-199-696_-199-695delinsC...