Canonical Allele Identifier: CA526973908
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs1188467486

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162115467_162115469del , CM000663.2:g.162115467_162115469del GRCh38
NC_000001.10:g.162085257_162085259del , CM000663.1:g.162085257_162085259del GRCh37
NC_000001.9:g.160351881_160351883del NCBI36
NG_015979.1:g.50677_50679del
NG_015979.2:g.50677_50679del

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.106-38938_106-38936del MANE Select ENSP00000355133.5:n.106-38938_106-38936de...
ENST00000361897.9:c.106-38938_106-38936del ENSP00000355133.5:n.106-38938_106-38936de...
ENST00000430120.3:c.106-38938_106-38936del ENSP00000396713.3:n.106-38938_106-38936de...
ENST00000530878.5:c.106-38938_106-38936del ENSP00000431586.1:n.106-38938_106-38936de...
NM_001164757.1:c.106-38938_106-38936del NP_001158229.1:n.106-38938_106-38936del
NM_014697.2:c.106-38938_106-38936del NP_055512.1:n.106-38938_106-38936del
XR_922217.1:n.884-1562_884-1560del
XR_922219.1:n.713-1562_713-1560del
XR_922221.1:n.713-8716_713-8714del
XR_002958375.1:n.3842-1562_3842-1560del
XR_002958378.1:n.3671-1562_3671-1560del
NM_014697.3:c.106-38938_106-38936del MANE Select NP_055512.1:n.106-38938_106-38936del
NM_001164757.2:c.106-38938_106-38936del NP_001158229.1:n.106-38938_106-38936del