Canonical Allele Identifier: CA2746398030

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199650_162199651insT , CM000663.2:g.162199650_162199651insT	GRCh38
NC_000001.10:g.162169440_162169441insT , CM000663.1:g.162169440_162169441insT	GRCh37
NC_000001.9:g.160436064_160436065insT	NCBI36
NG_015979.1:g.134860_134861insT
NG_015979.2:g.134860_134861insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.177+45174_177+45175insT MANE Select	ENSP00000355133.5:n.177+45174_177+45175insT
ENST00000361897.9:c.177+45174_177+45175insT	ENSP00000355133.5:n.177+45174_177+45175insT
ENST00000430120.3:c.177+45174_177+45175insT	ENSP00000396713.3:n.177+45174_177+45175insT
ENST00000530878.5:c.177+45174_177+45175insT	ENSP00000431586.1:n.177+45174_177+45175insT
NM_001164757.1:c.177+45174_177+45175insT	NP_001158229.1:n.177+45174_177+45175insT
NM_014697.2:c.177+45174_177+45175insT	NP_055512.1:n.177+45174_177+45175insT
NM_014697.3:c.177+45174_177+45175insT MANE Select	NP_055512.1:n.177+45174_177+45175insT
NM_001164757.2:c.177+45174_177+45175insT	NP_001158229.1:n.177+45174_177+45175insT