Canonical Allele Identifier: CA2746398018

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199602_162199608del , CM000663.2:g.162199602_162199608del	GRCh38
NC_000001.10:g.162169392_162169398del , CM000663.1:g.162169392_162169398del	GRCh37
NC_000001.9:g.160436016_160436022del	NCBI36
NG_015979.1:g.134812_134818del
NG_015979.2:g.134812_134818del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.177+45126_177+45132del MANE Select	ENSP00000355133.5:n.177+45126_177+45132del
ENST00000361897.9:c.177+45126_177+45132del	ENSP00000355133.5:n.177+45126_177+45132del
ENST00000430120.3:c.177+45126_177+45132del	ENSP00000396713.3:n.177+45126_177+45132del
ENST00000530878.5:c.177+45126_177+45132del	ENSP00000431586.1:n.177+45126_177+45132del
NM_001164757.1:c.177+45126_177+45132del	NP_001158229.1:n.177+45126_177+45132del
NM_014697.2:c.177+45126_177+45132del	NP_055512.1:n.177+45126_177+45132del
NM_014697.3:c.177+45126_177+45132del MANE Select	NP_055512.1:n.177+45126_177+45132del
NM_001164757.2:c.177+45126_177+45132del	NP_001158229.1:n.177+45126_177+45132del