Canonical Allele Identifier: CA727650912

Gene: NOS2

Linked Data

• dbSNP Id: rs1225113440
• MyVariant Identifiers: chr17:g.26111370_26111371del (hg19) ; chr17:g.27784344_27784345del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27784346_27784347del , CM000679.2:g.27784346_27784347del	GRCh38
NC_000017.10:g.26111372_26111373del , CM000679.1:g.26111372_26111373del	GRCh37
NC_000017.9:g.23135499_23135500del	NCBI36
NG_011470.1:g.21185_21186del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.319-1239_319-1238del	ENSP00000513259.1:n.319-1239_319-1238del
ENST00000697338.1:c.316-1239_316-1238del	ENSP00000513260.1:n.316-1239_316-1238del
ENST00000697339.1:c.315+4464_315+4465del	ENSP00000513261.1:n.315+4464_315+4465del
ENST00000697340.1:c.465-1239_465-1238del	ENSP00000513262.1:n.465-1239_465-1238del
ENST00000697341.1:n.438-1239_438-1238del
ENST00000313735.11:c.468-1239_468-1238del MANE Select	ENSP00000327251.6:n.468-1239_468-1238del
ENST00000646938.1:c.465-1239_465-1238del	ENSP00000494870.1:n.465-1239_465-1238del
ENST00000313735.10:c.468-1239_468-1238del	ENSP00000327251.6:n.468-1239_468-1238del
ENST00000621962.1:c.468-1239_468-1238del	ENSP00000482291.1:n.468-1239_468-1238del
NM_000625.4:c.468-1239_468-1238del MANE Select	NP_000616.3:n.468-1239_468-1238del
XM_011524859.1:c.468-1239_468-1238del	XP_011523161.1:n.468-1239_468-1238del
XM_011524860.1:c.465-1239_465-1238del	XP_011523162.1:n.465-1239_465-1238del
XM_011524861.1:c.468-1239_468-1238del	XP_011523163.1:n.468-1239_468-1238del
XM_011524862.1:c.-199-1239_-199-1238del	XP_011523164.1:n.-199-1239_-199-1238del