Canonical Allele Identifier: CA1008483626

Gene: NOS1AP

Linked Data

• gnomAD v3: 1-162199651-A-AGTGTGTGT
• gnomAD v4: 1-162199651-A-AGTGTGTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199651_162199652insGTGTGTGT , CM000663.2:g.162199651_162199652insGTGTGTGT	GRCh38
NC_000001.10:g.162169441_162169442insGTGTGTGT , CM000663.1:g.162169441_162169442insGTGTGTGT	GRCh37
NC_000001.9:g.160436065_160436066insGTGTGTGT	NCBI36
NG_015979.1:g.134861_134862insGTGTGTGT
NG_015979.2:g.134861_134862insGTGTGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.177+45175_177+45176insGTGTGTGT MANE Select	ENSP00000355133.5:n.177+45175_177+45176insGTGTGTGT
ENST00000361897.9:c.177+45175_177+45176insGTGTGTGT	ENSP00000355133.5:n.177+45175_177+45176insGTGTGTGT
ENST00000430120.3:c.177+45175_177+45176insGTGTGTGT	ENSP00000396713.3:n.177+45175_177+45176insGTGTGTGT
ENST00000530878.5:c.177+45175_177+45176insGTGTGTGT	ENSP00000431586.1:n.177+45175_177+45176insGTGTGTGT
NM_001164757.1:c.177+45175_177+45176insGTGTGTGT	NP_001158229.1:n.177+45175_177+45176insGTGTGTGT
NM_014697.2:c.177+45175_177+45176insGTGTGTGT	NP_055512.1:n.177+45175_177+45176insGTGTGTGT
NM_014697.3:c.177+45175_177+45176insGTGTGTGT MANE Select	NP_055512.1:n.177+45175_177+45176insGTGTGTGT
NM_001164757.2:c.177+45175_177+45176insGTGTGTGT	NP_001158229.1:n.177+45175_177+45176insGTGTGTGT