Canonical Allele Identifier: CA1140662038

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199647_162199650delinsTGTA , CM000663.2:g.162199647_162199650delinsTGTA	GRCh38
NC_000001.10:g.162169437_162169440delinsTGTA , CM000663.1:g.162169437_162169440delinsTGTA	GRCh37
NC_000001.9:g.160436061_160436064delinsTGTA	NCBI36
NG_015979.1:g.134857_134860delinsTGTA
NG_015979.2:g.134857_134860delinsTGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.177+45171_177+45174delinsTGTA MANE Select	ENSP00000355133.5:n.177+45171_177+45174delinsTGTA
ENST00000361897.9:c.177+45171_177+45174delinsTGTA	ENSP00000355133.5:n.177+45171_177+45174delinsTGTA
ENST00000430120.3:c.177+45171_177+45174delinsTGTA	ENSP00000396713.3:n.177+45171_177+45174delinsTGTA
ENST00000530878.5:c.177+45171_177+45174delinsTGTA	ENSP00000431586.1:n.177+45171_177+45174delinsTGTA
NM_001164757.1:c.177+45171_177+45174delinsTGTA	NP_001158229.1:n.177+45171_177+45174delinsTGTA
NM_014697.2:c.177+45171_177+45174delinsTGTA	NP_055512.1:n.177+45171_177+45174delinsTGTA
NM_014697.3:c.177+45171_177+45174delinsTGTA MANE Select	NP_055512.1:n.177+45171_177+45174delinsTGTA
NM_001164757.2:c.177+45171_177+45174delinsTGTA	NP_001158229.1:n.177+45171_177+45174delinsTGTA