Canonical Allele Identifier: CA2746398026

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199624_162199625insAGTG , CM000663.2:g.162199624_162199625insAGTG	GRCh38
NC_000001.10:g.162169414_162169415insAGTG , CM000663.1:g.162169414_162169415insAGTG	GRCh37
NC_000001.9:g.160436038_160436039insAGTG	NCBI36
NG_015979.1:g.134834_134835insAGTG
NG_015979.2:g.134834_134835insAGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.177+45148_177+45149insAGTG MANE Select	ENSP00000355133.5:n.177+45148_177+45149insAGTG
ENST00000361897.9:c.177+45148_177+45149insAGTG	ENSP00000355133.5:n.177+45148_177+45149insAGTG
ENST00000430120.3:c.177+45148_177+45149insAGTG	ENSP00000396713.3:n.177+45148_177+45149insAGTG
ENST00000530878.5:c.177+45148_177+45149insAGTG	ENSP00000431586.1:n.177+45148_177+45149insAGTG
NM_001164757.1:c.177+45148_177+45149insAGTG	NP_001158229.1:n.177+45148_177+45149insAGTG
NM_014697.2:c.177+45148_177+45149insAGTG	NP_055512.1:n.177+45148_177+45149insAGTG
NM_014697.3:c.177+45148_177+45149insAGTG MANE Select	NP_055512.1:n.177+45148_177+45149insAGTG
NM_001164757.2:c.177+45148_177+45149insAGTG	NP_001158229.1:n.177+45148_177+45149insAGTG