Canonical Allele Identifier: CA526974395
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs1375893875

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162116025_162116028del , CM000663.2:g.162116025_162116028del GRCh38
NC_000001.10:g.162085815_162085818del , CM000663.1:g.162085815_162085818del GRCh37
NC_000001.9:g.160352439_160352442del NCBI36
NG_015979.1:g.51235_51238del
NG_015979.2:g.51235_51238del

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.106-38380_106-38377del MANE Select ENSP00000355133.5:n.106-38380_106-38377de...
ENST00000361897.9:c.106-38380_106-38377del ENSP00000355133.5:n.106-38380_106-38377de...
ENST00000430120.3:c.106-38380_106-38377del ENSP00000396713.3:n.106-38380_106-38377de...
ENST00000530878.5:c.106-38380_106-38377del ENSP00000431586.1:n.106-38380_106-38377de...
NM_001164757.1:c.106-38380_106-38377del NP_001158229.1:n.106-38380_106-38377del
NM_014697.2:c.106-38380_106-38377del NP_055512.1:n.106-38380_106-38377del
XR_922217.1:n.884-2123_884-2120del
XR_922219.1:n.713-2123_713-2120del
XR_922221.1:n.713-9277_713-9274del
XR_002958375.1:n.3842-2123_3842-2120del
XR_002958378.1:n.3671-2123_3671-2120del
NM_014697.3:c.106-38380_106-38377del MANE Select NP_055512.1:n.106-38380_106-38377del
NM_001164757.2:c.106-38380_106-38377del NP_001158229.1:n.106-38380_106-38377del