Canonical Allele Identifier: CA890267961

Gene: NOS1AP

Linked Data

• dbSNP Id: rs1228247365
• gnomAD v3: 1-162199366-C-A
• gnomAD v4: 1-162199366-C-A
• MyVariant Identifiers: chr1:g.162169156C>A (hg19) ; chr1:g.162199366C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199366C>A , CM000663.2:g.162199366C>A	GRCh38
NC_000001.10:g.162169156C>A , CM000663.1:g.162169156C>A	GRCh37
NC_000001.9:g.160435780C>A	NCBI36
NG_015979.1:g.134576C>A
NG_015979.2:g.134576C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.177+44890C>A MANE Select	ENSP00000355133.5:n.177+44890C>A
ENST00000361897.9:c.177+44890C>A	ENSP00000355133.5:n.177+44890C>A
ENST00000430120.3:c.177+44890C>A	ENSP00000396713.3:n.177+44890C>A
ENST00000530878.5:c.177+44890C>A	ENSP00000431586.1:n.177+44890C>A
NM_001164757.1:c.177+44890C>A	NP_001158229.1:n.177+44890C>A
NM_014697.2:c.177+44890C>A	NP_055512.1:n.177+44890C>A
NM_014697.3:c.177+44890C>A MANE Select	NP_055512.1:n.177+44890C>A
NM_001164757.2:c.177+44890C>A	NP_001158229.1:n.177+44890C>A