Canonical Allele Identifier: CA526973887

Gene: NOS1AP

Linked Data

• dbSNP Id: rs1284433353
• gnomAD v2: 1-162085187-G-GTT
• gnomAD v3: 1-162115397-G-GTT
• gnomAD v4: 1-162115397-G-GTT
• MyVariant Identifiers: chr1:g.162085189_162085190insTT (hg19) ; chr1:g.162115399_162115400insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115409_162115410dup , CM000663.2:g.162115409_162115410dup	GRCh38
NC_000001.10:g.162085199_162085200dup , CM000663.1:g.162085199_162085200dup	GRCh37
NC_000001.9:g.160351823_160351824dup	NCBI36
NG_015979.1:g.50619_50620dup
NG_015979.2:g.50619_50620dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000361897.10:c.106-38996_106-38995dup MANE Select	ENSP00000355133.5:n.106-38996_106-38995dup
ENST00000361897.9:c.106-38996_106-38995dup	ENSP00000355133.5:n.106-38996_106-38995dup
ENST00000430120.3:c.106-38996_106-38995dup	ENSP00000396713.3:n.106-38996_106-38995dup
ENST00000530878.5:c.106-38996_106-38995dup	ENSP00000431586.1:n.106-38996_106-38995dup
NM_001164757.1:c.106-38996_106-38995dup	NP_001158229.1:n.106-38996_106-38995dup
NM_014697.2:c.106-38996_106-38995dup	NP_055512.1:n.106-38996_106-38995dup
XR_922217.1:n.884-1497_884-1496dup
XR_922219.1:n.713-1497_713-1496dup
XR_922221.1:n.713-8651_713-8650dup
XR_002958375.1:n.3842-1497_3842-1496dup
XR_002958378.1:n.3671-1497_3671-1496dup
NM_014697.3:c.106-38996_106-38995dup MANE Select	NP_055512.1:n.106-38996_106-38995dup
NM_001164757.2:c.106-38996_106-38995dup	NP_001158229.1:n.106-38996_106-38995dup