Canonical Allele Identifier: CA526980937
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs1354936296

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162199445_162199449del , CM000663.2:g.162199445_162199449del GRCh38
NC_000001.10:g.162169235_162169239del , CM000663.1:g.162169235_162169239del GRCh37
NC_000001.9:g.160435859_160435863del NCBI36
NG_015979.1:g.134655_134659del
NG_015979.2:g.134655_134659del

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.177+44969_177+44973del MANE Select ENSP00000355133.5:n.177+44969_177+44973de...
ENST00000361897.9:c.177+44969_177+44973del ENSP00000355133.5:n.177+44969_177+44973de...
ENST00000430120.3:c.177+44969_177+44973del ENSP00000396713.3:n.177+44969_177+44973de...
ENST00000530878.5:c.177+44969_177+44973del ENSP00000431586.1:n.177+44969_177+44973de...
NM_001164757.1:c.177+44969_177+44973del NP_001158229.1:n.177+44969_177+44973del
NM_014697.2:c.177+44969_177+44973del NP_055512.1:n.177+44969_177+44973del
NM_014697.3:c.177+44969_177+44973del MANE Select NP_055512.1:n.177+44969_177+44973del
NM_001164757.2:c.177+44969_177+44973del NP_001158229.1:n.177+44969_177+44973del