Canonical Allele Identifier: CA1008483475

Gene: NOS1AP

Linked Data

• dbSNP Id: rs1651922291
• gnomAD v3: 1-162199618-G-GTGTA
• gnomAD v4: 1-162199618-G-GTGTA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199621_162199622insATGT , CM000663.2:g.162199621_162199622insATGT	GRCh38
NC_000001.10:g.162169411_162169412insATGT , CM000663.1:g.162169411_162169412insATGT	GRCh37
NC_000001.9:g.160436035_160436036insATGT	NCBI36
NG_015979.1:g.134831_134832insATGT
NG_015979.2:g.134831_134832insATGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.177+45145_177+45146insATGT MANE Select	ENSP00000355133.5:n.177+45145_177+45146insATGT
ENST00000361897.9:c.177+45145_177+45146insATGT	ENSP00000355133.5:n.177+45145_177+45146insATGT
ENST00000430120.3:c.177+45145_177+45146insATGT	ENSP00000396713.3:n.177+45145_177+45146insATGT
ENST00000530878.5:c.177+45145_177+45146insATGT	ENSP00000431586.1:n.177+45145_177+45146insATGT
NM_001164757.1:c.177+45145_177+45146insATGT	NP_001158229.1:n.177+45145_177+45146insATGT
NM_014697.2:c.177+45145_177+45146insATGT	NP_055512.1:n.177+45145_177+45146insATGT
NM_014697.3:c.177+45145_177+45146insATGT MANE Select	NP_055512.1:n.177+45145_177+45146insATGT
NM_001164757.2:c.177+45145_177+45146insATGT	NP_001158229.1:n.177+45145_177+45146insATGT