Canonical Allele Identifier: CA2254015179

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27784513_27784515delinsAAC , CM000679.2:g.27784513_27784515delinsAAC	GRCh38
NC_000017.10:g.26111539_26111541delinsAAC , CM000679.1:g.26111539_26111541delinsAAC	GRCh37
NC_000017.9:g.23135666_23135668delinsAAC	NCBI36
NG_011470.1:g.21015_21017delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.319-1409_319-1407delinsGTT	ENSP00000513259.1:n.319-1409_319-1407delinsGTT
ENST00000697338.1:c.316-1409_316-1407delinsGTT	ENSP00000513260.1:n.316-1409_316-1407delinsGTT
ENST00000697339.1:c.315+4294_315+4296delinsGTT	ENSP00000513261.1:n.315+4294_315+4296delinsGTT
ENST00000697340.1:c.465-1409_465-1407delinsGTT	ENSP00000513262.1:n.465-1409_465-1407delinsGTT
ENST00000697341.1:n.438-1409_438-1407delinsGTT
ENST00000313735.11:c.468-1409_468-1407delinsGTT MANE Select	ENSP00000327251.6:n.468-1409_468-1407delinsGTT
ENST00000646938.1:c.465-1409_465-1407delinsGTT	ENSP00000494870.1:n.465-1409_465-1407delinsGTT
ENST00000313735.10:c.468-1409_468-1407delinsGTT	ENSP00000327251.6:n.468-1409_468-1407delinsGTT
ENST00000621962.1:c.468-1409_468-1407delinsGTT	ENSP00000482291.1:n.468-1409_468-1407delinsGTT
NM_000625.4:c.468-1409_468-1407delinsGTT MANE Select	NP_000616.3:n.468-1409_468-1407delinsGTT
XM_011524859.1:c.468-1409_468-1407delinsGTT	XP_011523161.1:n.468-1409_468-1407delinsGTT
XM_011524860.1:c.465-1409_465-1407delinsGTT	XP_011523162.1:n.465-1409_465-1407delinsGTT
XM_011524861.1:c.468-1409_468-1407delinsGTT	XP_011523163.1:n.468-1409_468-1407delinsGTT
XM_011524862.1:c.-199-1409_-199-1407delinsGTT	XP_011523164.1:n.-199-1409_-199-1407delinsGTT