Canonical Allele Identifier: CA31618819

Gene: NOS1AP

Linked Data

• dbSNP Id: rs1021613074
• gnomAD v3: 1-162115829-G-A
• gnomAD v4: 1-162115829-G-A
• MyVariant Identifiers: chr1:g.162085619G>A (hg19) ; chr1:g.162115829G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115829G>A , CM000663.2:g.162115829G>A	GRCh38
NC_000001.10:g.162085619G>A , CM000663.1:g.162085619G>A	GRCh37
NC_000001.9:g.160352243G>A	NCBI36
NG_015979.1:g.51039G>A
NG_015979.2:g.51039G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000361897.10:c.106-38576G>A MANE Select	ENSP00000355133.5:n.106-38576G>A
ENST00000361897.9:c.106-38576G>A	ENSP00000355133.5:n.106-38576G>A
ENST00000430120.3:c.106-38576G>A	ENSP00000396713.3:n.106-38576G>A
ENST00000530878.5:c.106-38576G>A	ENSP00000431586.1:n.106-38576G>A
NM_001164757.1:c.106-38576G>A	NP_001158229.1:n.106-38576G>A
NM_014697.2:c.106-38576G>A	NP_055512.1:n.106-38576G>A
XR_922217.1:n.884-1927C>T
XR_922219.1:n.713-1927C>T
XR_922221.1:n.713-9081C>T
XR_002958375.1:n.3842-1927C>T
XR_002958378.1:n.3671-1927C>T
NM_014697.3:c.106-38576G>A MANE Select	NP_055512.1:n.106-38576G>A
NM_001164757.2:c.106-38576G>A	NP_001158229.1:n.106-38576G>A