Canonical Allele Identifier: CA1203049893

Gene: NOS1AP

Linked Data

• dbSNP Id: rs1651924814

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199637_162199638insCT , CM000663.2:g.162199637_162199638insCT	GRCh38
NC_000001.10:g.162169427_162169428insCT , CM000663.1:g.162169427_162169428insCT	GRCh37
NC_000001.9:g.160436051_160436052insCT	NCBI36
NG_015979.1:g.134847_134848insCT
NG_015979.2:g.134847_134848insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.177+45161_177+45162insCT MANE Select	ENSP00000355133.5:n.177+45161_177+45162insCT
ENST00000361897.9:c.177+45161_177+45162insCT	ENSP00000355133.5:n.177+45161_177+45162insCT
ENST00000430120.3:c.177+45161_177+45162insCT	ENSP00000396713.3:n.177+45161_177+45162insCT
ENST00000530878.5:c.177+45161_177+45162insCT	ENSP00000431586.1:n.177+45161_177+45162insCT
NM_001164757.1:c.177+45161_177+45162insCT	NP_001158229.1:n.177+45161_177+45162insCT
NM_014697.2:c.177+45161_177+45162insCT	NP_055512.1:n.177+45161_177+45162insCT
NM_014697.3:c.177+45161_177+45162insCT MANE Select	NP_055512.1:n.177+45161_177+45162insCT
NM_001164757.2:c.177+45161_177+45162insCT	NP_001158229.1:n.177+45161_177+45162insCT