Canonical Allele Identifier: CA1203049856

Gene: NOS1AP

Linked Data

• dbSNP Id: rs1651922360

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199625_162199626insCTGTGTGT , CM000663.2:g.162199625_162199626insCTGTGTGT	GRCh38
NC_000001.10:g.162169415_162169416insCTGTGTGT , CM000663.1:g.162169415_162169416insCTGTGTGT	GRCh37
NC_000001.9:g.160436039_160436040insCTGTGTGT	NCBI36
NG_015979.1:g.134835_134836insCTGTGTGT
NG_015979.2:g.134835_134836insCTGTGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.177+45149_177+45150insCTGTGTGT MANE Select	ENSP00000355133.5:n.177+45149_177+45150insCTGTGTGT
ENST00000361897.9:c.177+45149_177+45150insCTGTGTGT	ENSP00000355133.5:n.177+45149_177+45150insCTGTGTGT
ENST00000430120.3:c.177+45149_177+45150insCTGTGTGT	ENSP00000396713.3:n.177+45149_177+45150insCTGTGTGT
ENST00000530878.5:c.177+45149_177+45150insCTGTGTGT	ENSP00000431586.1:n.177+45149_177+45150insCTGTGTGT
NM_001164757.1:c.177+45149_177+45150insCTGTGTGT	NP_001158229.1:n.177+45149_177+45150insCTGTGTGT
NM_014697.2:c.177+45149_177+45150insCTGTGTGT	NP_055512.1:n.177+45149_177+45150insCTGTGTGT
NM_014697.3:c.177+45149_177+45150insCTGTGTGT MANE Select	NP_055512.1:n.177+45149_177+45150insCTGTGTGT
NM_001164757.2:c.177+45149_177+45150insCTGTGTGT	NP_001158229.1:n.177+45149_177+45150insCTGTGTGT