Canonical Allele Identifier: CA2605255968

Gene: NOS1AP

Linked Data

• gnomAD v3: 1-162199624-G-GTGTC
• gnomAD v4: 1-162199624-G-GTGTC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199627_162199628insCTGT , CM000663.2:g.162199627_162199628insCTGT	GRCh38
NC_000001.10:g.162169417_162169418insCTGT , CM000663.1:g.162169417_162169418insCTGT	GRCh37
NC_000001.9:g.160436041_160436042insCTGT	NCBI36
NG_015979.1:g.134837_134838insCTGT
NG_015979.2:g.134837_134838insCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.177+45151_177+45152insCTGT MANE Select	ENSP00000355133.5:n.177+45151_177+45152insCTGT
ENST00000361897.9:c.177+45151_177+45152insCTGT	ENSP00000355133.5:n.177+45151_177+45152insCTGT
ENST00000430120.3:c.177+45151_177+45152insCTGT	ENSP00000396713.3:n.177+45151_177+45152insCTGT
ENST00000530878.5:c.177+45151_177+45152insCTGT	ENSP00000431586.1:n.177+45151_177+45152insCTGT
NM_001164757.1:c.177+45151_177+45152insCTGT	NP_001158229.1:n.177+45151_177+45152insCTGT
NM_014697.2:c.177+45151_177+45152insCTGT	NP_055512.1:n.177+45151_177+45152insCTGT
NM_014697.3:c.177+45151_177+45152insCTGT MANE Select	NP_055512.1:n.177+45151_177+45152insCTGT
NM_001164757.2:c.177+45151_177+45152insCTGT	NP_001158229.1:n.177+45151_177+45152insCTGT