Canonical Allele Identifier: CA2254006479

Gene: NOS2

Linked Data

• dbSNP Id: rs1908248374

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27764930_27764931del , CM000679.2:g.27764930_27764931del	GRCh38
NC_000017.10:g.26091956_26091957del , CM000679.1:g.26091956_26091957del	GRCh37
NC_000017.9:g.23116083_23116084del	NCBI36
NG_011470.1:g.40600_40601del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*3092+677_*3092+678del	ENSP00000513259.1:n.*3092+677_*3092+678del
ENST00000697338.1:c.2276+605_2276+606del	ENSP00000513260.1:n.2276+605_2276+606del
ENST00000697339.1:c.1390+677_1390+678del	ENSP00000513261.1:n.1390+677_1390+678del
ENST00000697340.1:c.*1145+605_*1145+606del	ENSP00000513262.1:n.*1145+605_*1145+606del
ENST00000697341.1:n.2398+605_2398+606del
ENST00000313735.11:c.2428+605_2428+606del MANE Select	ENSP00000327251.6:n.2428+605_2428+606del
ENST00000646938.1:c.2425+605_2425+606del	ENSP00000494870.1:n.2425+605_2425+606del
ENST00000313735.10:c.2428+605_2428+606del	ENSP00000327251.6:n.2428+605_2428+606del
ENST00000621962.1:c.2311+605_2311+606del	ENSP00000482291.1:n.2311+605_2311+606del
NM_000625.4:c.2428+605_2428+606del MANE Select	NP_000616.3:n.2428+605_2428+606del
XM_011524859.1:c.2428+605_2428+606del	XP_011523161.1:n.2428+605_2428+606del
XM_011524860.1:c.2425+605_2425+606del	XP_011523162.1:n.2425+605_2425+606del
XM_011524861.1:c.2356+677_2356+678del	XP_011523163.1:n.2356+677_2356+678del
XM_011524862.1:c.1762+605_1762+606del	XP_011523164.1:n.1762+605_1762+606del