Canonical Allele Identifier: CA2254014905

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27783899_27783932delinsAGCCTGGTCAAGCCAGGACTGGGACCTGGCTATC , CM000679.2:g.27783899_27783932delinsAGCCTGGTCAAGCCAGGACTGGGACCTGGCTATC	GRCh38
NC_000017.10:g.26110925_26110958delinsAGCCTGGTCAAGCCAGGACTGGGACCTGGCTATC , CM000679.1:g.26110925_26110958delinsAGCCTGGTCAAGCCAGGACTGGGACCTGGCTATC	GRCh37
NC_000017.9:g.23135052_23135085delinsAGCCTGGTCAAGCCAGGACTGGGACCTGGCTATC	NCBI36
NG_011470.1:g.21598_21631delinsGATAGCCAGGTCCCAGTCCTGGCTTGACCAGGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.319-826_319-793delinsGATAGCCAGGTCCCAGTCCTGGCTTGACCAGGCT	ENSP00000513259.1:n.319-826_319-793delinsGATAGCCAGGTCCCAGTCCT...
ENST00000697338.1:c.316-826_316-793delinsGATAGCCAGGTCCCAGTCCTGGCTTGACCAGGCT	ENSP00000513260.1:n.316-826_316-793delinsGATAGCCAGGTCCCAGTCCT...
ENST00000697339.1:c.315+4877_315+4910delinsGATAGCCAGGTCCCAGTCCTGGCTTGACCAGGCT	ENSP00000513261.1:n.315+4877_315+4910delinsGATAGCCAGGTCCCAGTC...
ENST00000697340.1:c.465-826_465-793delinsGATAGCCAGGTCCCAGTCCTGGCTTGACCAGGCT	ENSP00000513262.1:n.465-826_465-793delinsGATAGCCAGGTCCCAGTCCT...
ENST00000697341.1:n.438-826_438-793delinsGATAGCCAGGTCCCAGTCCTGGCTTGACCAGGCT
ENST00000313735.11:c.468-826_468-793delinsGATAGCCAGGTCCCAGTCCTGGCTTGACCAGGCT MANE Select	ENSP00000327251.6:n.468-826_468-793delinsGATAGCCAGGTCCCAGTCCT...
ENST00000646938.1:c.465-826_465-793delinsGATAGCCAGGTCCCAGTCCTGGCTTGACCAGGCT	ENSP00000494870.1:n.465-826_465-793delinsGATAGCCAGGTCCCAGTCCT...
ENST00000313735.10:c.468-826_468-793delinsGATAGCCAGGTCCCAGTCCTGGCTTGACCAGGCT	ENSP00000327251.6:n.468-826_468-793delinsGATAGCCAGGTCCCAGTCCT...
ENST00000621962.1:c.468-826_468-793delinsGATAGCCAGGTCCCAGTCCTGGCTTGACCAGGCT	ENSP00000482291.1:n.468-826_468-793delinsGATAGCCAGGTCCCAGTCCT...
NM_000625.4:c.468-826_468-793delinsGATAGCCAGGTCCCAGTCCTGGCTTGACCAGGCT MANE Select	NP_000616.3:n.468-826_468-793delinsGATAGCCAGGTCCCAGTCCTGGCTTG...
XM_011524859.1:c.468-826_468-793delinsGATAGCCAGGTCCCAGTCCTGGCTTGACCAGGCT	XP_011523161.1:n.468-826_468-793delinsGATAGCCAGGTCCCAGTCCTGGC...
XM_011524860.1:c.465-826_465-793delinsGATAGCCAGGTCCCAGTCCTGGCTTGACCAGGCT	XP_011523162.1:n.465-826_465-793delinsGATAGCCAGGTCCCAGTCCTGGC...
XM_011524861.1:c.468-826_468-793delinsGATAGCCAGGTCCCAGTCCTGGCTTGACCAGGCT	XP_011523163.1:n.468-826_468-793delinsGATAGCCAGGTCCCAGTCCTGGC...
XM_011524862.1:c.-199-826_-199-793delinsGATAGCCAGGTCCCAGTCCTGGCTTGACCAGGCT	XP_011523164.1:n.-199-826_-199-793delinsGATAGCCAGGTCCCAGTCCTG...