Canonical Allele Identifier: CA2838214867

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162251741G>A , CM000663.2:g.162251741G>A	GRCh38
NC_000001.10:g.162221531G>A , CM000663.1:g.162221531G>A	GRCh37
NC_000001.9:g.160488155G>A	NCBI36
NG_015979.1:g.186951G>A
NG_015979.2:g.186951G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.178-35603G>A MANE Select	ENSP00000355133.5:n.178-35603G>A
ENST00000361897.9:c.178-35603G>A	ENSP00000355133.5:n.178-35603G>A
ENST00000430120.3:c.178-35603G>A	ENSP00000396713.3:n.178-35603G>A
ENST00000530878.5:c.178-35603G>A	ENSP00000431586.1:n.178-35603G>A
NM_001164757.1:c.178-35603G>A	NP_001158229.1:n.178-35603G>A
NM_014697.2:c.178-35603G>A	NP_055512.1:n.178-35603G>A
NM_014697.3:c.178-35603G>A MANE Select	NP_055512.1:n.178-35603G>A
NM_001164757.2:c.178-35603G>A	NP_001158229.1:n.178-35603G>A