Canonical Allele Identifier: CA890267991

Gene: NOS1AP

Linked Data

• dbSNP Id: rs1425155802
• gnomAD v3: 1-162199563-C-A
• gnomAD v4: 1-162199563-C-A
• MyVariant Identifiers: chr1:g.162169353C>A (hg19) ; chr1:g.162199563C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199563C>A , CM000663.2:g.162199563C>A	GRCh38
NC_000001.10:g.162169353C>A , CM000663.1:g.162169353C>A	GRCh37
NC_000001.9:g.160435977C>A	NCBI36
NG_015979.1:g.134773C>A
NG_015979.2:g.134773C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.177+45087C>A MANE Select	ENSP00000355133.5:n.177+45087C>A
ENST00000361897.9:c.177+45087C>A	ENSP00000355133.5:n.177+45087C>A
ENST00000430120.3:c.177+45087C>A	ENSP00000396713.3:n.177+45087C>A
ENST00000530878.5:c.177+45087C>A	ENSP00000431586.1:n.177+45087C>A
NM_001164757.1:c.177+45087C>A	NP_001158229.1:n.177+45087C>A
NM_014697.2:c.177+45087C>A	NP_055512.1:n.177+45087C>A
NM_014697.3:c.177+45087C>A MANE Select	NP_055512.1:n.177+45087C>A
NM_001164757.2:c.177+45087C>A	NP_001158229.1:n.177+45087C>A