Canonical Allele Identifier: CA1008481763

Gene: NOS1AP

Linked Data

• gnomAD v3: 1-162254802-A-G
• gnomAD v4: 1-162254802-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162254802A>G , CM000663.2:g.162254802A>G	GRCh38
NC_000001.10:g.162224592A>G , CM000663.1:g.162224592A>G	GRCh37
NC_000001.9:g.160491216A>G	NCBI36
NG_015979.1:g.190012A>G
NG_015979.2:g.190012A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361897.10:c.178-32542A>G MANE Select	ENSP00000355133.5:n.178-32542A>G
ENST00000361897.9:c.178-32542A>G	ENSP00000355133.5:n.178-32542A>G
ENST00000430120.3:c.178-32542A>G	ENSP00000396713.3:n.178-32542A>G
ENST00000530878.5:c.178-32542A>G	ENSP00000431586.1:n.178-32542A>G
NM_001164757.1:c.178-32542A>G	NP_001158229.1:n.178-32542A>G
NM_014697.2:c.178-32542A>G	NP_055512.1:n.178-32542A>G
NM_014697.3:c.178-32542A>G MANE Select	NP_055512.1:n.178-32542A>G
NM_001164757.2:c.178-32542A>G	NP_001158229.1:n.178-32542A>G