Canonical Allele Identifier: CA1008480555
Gene: NOS1AP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162115306_162115307insACCATTACTAGT , CM000663.2:g.162115306_162115307insACCATTACTAGT GRCh38
NC_000001.10:g.162085096_162085097insACCATTACTAGT , CM000663.1:g.162085096_162085097insACCATTACTAGT GRCh37
NC_000001.9:g.160351720_160351721insACCATTACTAGT NCBI36
NG_015979.1:g.50516_50517insACCATTACTAGT
NG_015979.2:g.50516_50517insACCATTACTAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000361897.10:c.106-39099_106-39098insACCATTACTAGT MANE Select ENSP00000355133.5:n.106-39099_106-39098insACCATTACTAGT
ENST00000361897.9:c.106-39099_106-39098insACCATTACTAGT ENSP00000355133.5:n.106-39099_106-39098insACCATTACTAGT
ENST00000430120.3:c.106-39099_106-39098insACCATTACTAGT ENSP00000396713.3:n.106-39099_106-39098insACCATTACTAGT
ENST00000530878.5:c.106-39099_106-39098insACCATTACTAGT ENSP00000431586.1:n.106-39099_106-39098insACCATTACTAGT
NM_001164757.1:c.106-39099_106-39098insACCATTACTAGT NP_001158229.1:n.106-39099_106-39098insACCATTACTAGT
NM_014697.2:c.106-39099_106-39098insACCATTACTAGT NP_055512.1:n.106-39099_106-39098insACCATTACTAGT
XR_922217.1:n.884-1405_884-1404insACTAGTAATGGT
XR_922219.1:n.713-1405_713-1404insACTAGTAATGGT
XR_922221.1:n.713-8559_713-8558insACTAGTAATGGT
XR_002958375.1:n.3842-1405_3842-1404insACTAGTAATGGT
XR_002958378.1:n.3671-1405_3671-1404insACTAGTAATGGT
NM_014697.3:c.106-39099_106-39098insACCATTACTAGT MANE Select NP_055512.1:n.106-39099_106-39098insACCATTACTAGT
NM_001164757.2:c.106-39099_106-39098insACCATTACTAGT NP_001158229.1:n.106-39099_106-39098insACCATTACTAGT