Canonical Allele Identifier: CA31691999

Gene: NOS1AP

Linked Data

• dbSNP Id: rs775603474

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199645_162199646insCT , CM000663.2:g.162199645_162199646insCT	GRCh38
NC_000001.10:g.162169435_162169436insCT , CM000663.1:g.162169435_162169436insCT	GRCh37
NC_000001.9:g.160436059_160436060insCT	NCBI36
NG_015979.1:g.134855_134856insCT
NG_015979.2:g.134855_134856insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.177+45169_177+45170insCT MANE Select	ENSP00000355133.5:n.177+45169_177+45170insCT
ENST00000361897.9:c.177+45169_177+45170insCT	ENSP00000355133.5:n.177+45169_177+45170insCT
ENST00000430120.3:c.177+45169_177+45170insCT	ENSP00000396713.3:n.177+45169_177+45170insCT
ENST00000530878.5:c.177+45169_177+45170insCT	ENSP00000431586.1:n.177+45169_177+45170insCT
NM_001164757.1:c.177+45169_177+45170insCT	NP_001158229.1:n.177+45169_177+45170insCT
NM_014697.2:c.177+45169_177+45170insCT	NP_055512.1:n.177+45169_177+45170insCT
NM_014697.3:c.177+45169_177+45170insCT MANE Select	NP_055512.1:n.177+45169_177+45170insCT
NM_001164757.2:c.177+45169_177+45170insCT	NP_001158229.1:n.177+45169_177+45170insCT