Canonical Allele Identifier: CA1008483624

Gene: NOS1AP

Linked Data

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

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199651_162199652insGTGT , CM000663.2:g.162199651_162199652insGTGT	GRCh38
NC_000001.10:g.162169441_162169442insGTGT , CM000663.1:g.162169441_162169442insGTGT	GRCh37
NC_000001.9:g.160436065_160436066insGTGT	NCBI36
NG_015979.1:g.134861_134862insGTGT
NG_015979.2:g.134861_134862insGTGT

Transcript Alleles

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