Canonical Allele Identifier: CA1203016961

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115615_162115616delinsTC , CM000663.2:g.162115615_162115616delinsTC	GRCh38
NC_000001.10:g.162085405_162085406delinsTC , CM000663.1:g.162085405_162085406delinsTC	GRCh37
NC_000001.9:g.160352029_160352030delinsTC	NCBI36
NG_015979.1:g.50825_50826delinsTC
NG_015979.2:g.50825_50826delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.106-38790_106-38789delinsTC MANE Select	ENSP00000355133.5:n.106-38790_106-38789delinsTC
ENST00000361897.9:c.106-38790_106-38789delinsTC	ENSP00000355133.5:n.106-38790_106-38789delinsTC
ENST00000430120.3:c.106-38790_106-38789delinsTC	ENSP00000396713.3:n.106-38790_106-38789delinsTC
ENST00000530878.5:c.106-38790_106-38789delinsTC	ENSP00000431586.1:n.106-38790_106-38789delinsTC
NM_001164757.1:c.106-38790_106-38789delinsTC	NP_001158229.1:n.106-38790_106-38789delinsTC
NM_014697.2:c.106-38790_106-38789delinsTC	NP_055512.1:n.106-38790_106-38789delinsTC
XR_922217.1:n.884-1714_884-1713delinsGA
XR_922219.1:n.713-1714_713-1713delinsGA
XR_922221.1:n.713-8868_713-8867delinsGA
XR_002958375.1:n.3842-1714_3842-1713delinsGA
XR_002958378.1:n.3671-1714_3671-1713delinsGA
NM_014697.3:c.106-38790_106-38789delinsTC MANE Select	NP_055512.1:n.106-38790_106-38789delinsTC
NM_001164757.2:c.106-38790_106-38789delinsTC	NP_001158229.1:n.106-38790_106-38789delinsTC