Canonical Allele Identifier: CA1203016889

Gene: NOS1AP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115433_162115434delinsGT , CM000663.2:g.162115433_162115434delinsGT	GRCh38
NC_000001.10:g.162085223_162085224delinsGT , CM000663.1:g.162085223_162085224delinsGT	GRCh37
NC_000001.9:g.160351847_160351848delinsGT	NCBI36
NG_015979.1:g.50643_50644delinsGT
NG_015979.2:g.50643_50644delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361897.10:c.106-38972_106-38971delinsGT MANE Select	ENSP00000355133.5:n.106-38972_106-38971delinsGT
ENST00000361897.9:c.106-38972_106-38971delinsGT	ENSP00000355133.5:n.106-38972_106-38971delinsGT
ENST00000430120.3:c.106-38972_106-38971delinsGT	ENSP00000396713.3:n.106-38972_106-38971delinsGT
ENST00000530878.5:c.106-38972_106-38971delinsGT	ENSP00000431586.1:n.106-38972_106-38971delinsGT
NM_001164757.1:c.106-38972_106-38971delinsGT	NP_001158229.1:n.106-38972_106-38971delinsGT
NM_014697.2:c.106-38972_106-38971delinsGT	NP_055512.1:n.106-38972_106-38971delinsGT
XR_922217.1:n.884-1532_884-1531delinsAC
XR_922219.1:n.713-1532_713-1531delinsAC
XR_922221.1:n.713-8686_713-8685delinsAC
XR_002958375.1:n.3842-1532_3842-1531delinsAC
XR_002958378.1:n.3671-1532_3671-1531delinsAC
NM_014697.3:c.106-38972_106-38971delinsGT MANE Select	NP_055512.1:n.106-38972_106-38971delinsGT
NM_001164757.2:c.106-38972_106-38971delinsGT	NP_001158229.1:n.106-38972_106-38971delinsGT