Canonical Allele Identifier: CA1203071623
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs1653978584
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162254958_162254959del , CM000663.2:g.162254958_162254959del GRCh38
NC_000001.10:g.162224748_162224749del , CM000663.1:g.162224748_162224749del GRCh37
NC_000001.9:g.160491372_160491373del NCBI36
NG_015979.1:g.190168_190169del
NG_015979.2:g.190168_190169del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361897.10:c.178-32386_178-32385del MANE Select ENSP00000355133.5:n.178-32386_178-32385del
ENST00000361897.9:c.178-32386_178-32385del ENSP00000355133.5:n.178-32386_178-32385del
ENST00000430120.3:c.178-32386_178-32385del ENSP00000396713.3:n.178-32386_178-32385del
ENST00000530878.5:c.178-32386_178-32385del ENSP00000431586.1:n.178-32386_178-32385del
NM_001164757.1:c.178-32386_178-32385del NP_001158229.1:n.178-32386_178-32385del
NM_014697.2:c.178-32386_178-32385del NP_055512.1:n.178-32386_178-32385del
NM_014697.3:c.178-32386_178-32385del MANE Select NP_055512.1:n.178-32386_178-32385del
NM_001164757.2:c.178-32386_178-32385del NP_001158229.1:n.178-32386_178-32385del
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