Canonical Allele Identifier: CA31618475

Gene: NOS1AP

Linked Data

• dbSNP Id: rs895971205
• gnomAD v3: 1-162115410-T-A
• gnomAD v4: 1-162115410-T-A
• MyVariant Identifiers: chr1:g.162085200T>A (hg19) ; chr1:g.162115410T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115410T>A , CM000663.2:g.162115410T>A	GRCh38
NC_000001.10:g.162085200T>A , CM000663.1:g.162085200T>A	GRCh37
NC_000001.9:g.160351824T>A	NCBI36
NG_015979.1:g.50620T>A
NG_015979.2:g.50620T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.106-38995T>A MANE Select	ENSP00000355133.5:n.106-38995T>A
ENST00000361897.9:c.106-38995T>A	ENSP00000355133.5:n.106-38995T>A
ENST00000430120.3:c.106-38995T>A	ENSP00000396713.3:n.106-38995T>A
ENST00000530878.5:c.106-38995T>A	ENSP00000431586.1:n.106-38995T>A
NM_001164757.1:c.106-38995T>A	NP_001158229.1:n.106-38995T>A
NM_014697.2:c.106-38995T>A	NP_055512.1:n.106-38995T>A
XR_922217.1:n.884-1508A>T
XR_922219.1:n.713-1508A>T
XR_922221.1:n.713-8662A>T
XR_002958375.1:n.3842-1508A>T
XR_002958378.1:n.3671-1508A>T
NM_014697.3:c.106-38995T>A MANE Select	NP_055512.1:n.106-38995T>A
NM_001164757.2:c.106-38995T>A	NP_001158229.1:n.106-38995T>A