Canonical Allele Identifier: CA1203017106
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs1647933861

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162115993_162115996del , CM000663.2:g.162115993_162115996del GRCh38
NC_000001.10:g.162085783_162085786del , CM000663.1:g.162085783_162085786del GRCh37
NC_000001.9:g.160352407_160352410del NCBI36
NG_015979.1:g.51203_51206del
NG_015979.2:g.51203_51206del

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.106-38412_106-38409del MANE Select ENSP00000355133.5:n.106-38412_106-38409de...
ENST00000361897.9:c.106-38412_106-38409del ENSP00000355133.5:n.106-38412_106-38409de...
ENST00000430120.3:c.106-38412_106-38409del ENSP00000396713.3:n.106-38412_106-38409de...
ENST00000530878.5:c.106-38412_106-38409del ENSP00000431586.1:n.106-38412_106-38409de...
NM_001164757.1:c.106-38412_106-38409del NP_001158229.1:n.106-38412_106-38409del
NM_014697.2:c.106-38412_106-38409del NP_055512.1:n.106-38412_106-38409del
XR_922217.1:n.884-2091_884-2088del
XR_922219.1:n.713-2091_713-2088del
XR_922221.1:n.713-9245_713-9242del
XR_002958375.1:n.3842-2091_3842-2088del
XR_002958378.1:n.3671-2091_3671-2088del
NM_014697.3:c.106-38412_106-38409del MANE Select NP_055512.1:n.106-38412_106-38409del
NM_001164757.2:c.106-38412_106-38409del NP_001158229.1:n.106-38412_106-38409del