Canonical Allele Identifier: CA2254006619

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27765231_27765232delinsAC , CM000679.2:g.27765231_27765232delinsAC	GRCh38
NC_000017.10:g.26092257_26092258delinsAC , CM000679.1:g.26092257_26092258delinsAC	GRCh37
NC_000017.9:g.23116384_23116385delinsAC	NCBI36
NG_011470.1:g.40298_40299delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*3092+375_*3092+376delinsGT	ENSP00000513259.1:n.*3092+375_*3092+376delinsGT
ENST00000697338.1:c.2276+303_2276+304delinsGT	ENSP00000513260.1:n.2276+303_2276+304delinsGT
ENST00000697339.1:c.1390+375_1390+376delinsGT	ENSP00000513261.1:n.1390+375_1390+376delinsGT
ENST00000697340.1:c.*1145+303_*1145+304delinsGT	ENSP00000513262.1:n.*1145+303_*1145+304delinsGT
ENST00000697341.1:n.2398+303_2398+304delinsGT
ENST00000313735.11:c.2428+303_2428+304delinsGT MANE Select	ENSP00000327251.6:n.2428+303_2428+304delinsGT
ENST00000646938.1:c.2425+303_2425+304delinsGT	ENSP00000494870.1:n.2425+303_2425+304delinsGT
ENST00000313735.10:c.2428+303_2428+304delinsGT	ENSP00000327251.6:n.2428+303_2428+304delinsGT
ENST00000621962.1:c.2311+303_2311+304delinsGT	ENSP00000482291.1:n.2311+303_2311+304delinsGT
NM_000625.4:c.2428+303_2428+304delinsGT MANE Select	NP_000616.3:n.2428+303_2428+304delinsGT
XM_011524859.1:c.2428+303_2428+304delinsGT	XP_011523161.1:n.2428+303_2428+304delinsGT
XM_011524860.1:c.2425+303_2425+304delinsGT	XP_011523162.1:n.2425+303_2425+304delinsGT
XM_011524861.1:c.2356+375_2356+376delinsGT	XP_011523163.1:n.2356+375_2356+376delinsGT
XM_011524862.1:c.1762+303_1762+304delinsGT	XP_011523164.1:n.1762+303_1762+304delinsGT