Canonical Allele Identifier: CA1203049887

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162199635_162199636delinsTG , CM000663.2:g.162199635_162199636delinsTG	GRCh38
NC_000001.10:g.162169425_162169426delinsTG , CM000663.1:g.162169425_162169426delinsTG	GRCh37
NC_000001.9:g.160436049_160436050delinsTG	NCBI36
NG_015979.1:g.134845_134846delinsTG
NG_015979.2:g.134845_134846delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.177+45159_177+45160delinsTG MANE Select	ENSP00000355133.5:n.177+45159_177+45160delinsTG
ENST00000361897.9:c.177+45159_177+45160delinsTG	ENSP00000355133.5:n.177+45159_177+45160delinsTG
ENST00000430120.3:c.177+45159_177+45160delinsTG	ENSP00000396713.3:n.177+45159_177+45160delinsTG
ENST00000530878.5:c.177+45159_177+45160delinsTG	ENSP00000431586.1:n.177+45159_177+45160delinsTG
NM_001164757.1:c.177+45159_177+45160delinsTG	NP_001158229.1:n.177+45159_177+45160delinsTG
NM_014697.2:c.177+45159_177+45160delinsTG	NP_055512.1:n.177+45159_177+45160delinsTG
NM_014697.3:c.177+45159_177+45160delinsTG MANE Select	NP_055512.1:n.177+45159_177+45160delinsTG
NM_001164757.2:c.177+45159_177+45160delinsTG	NP_001158229.1:n.177+45159_177+45160delinsTG