Canonical Allele Identifier: CA31691736
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs541488806

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162199381A>G , CM000663.2:g.162199381A>G GRCh38
NC_000001.10:g.162169171A>G , CM000663.1:g.162169171A>G GRCh37
NC_000001.9:g.160435795A>G NCBI36
NG_015979.1:g.134591A>G
NG_015979.2:g.134591A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.177+44905A>G MANE Select ENSP00000355133.5:n.177+44905A>G
ENST00000361897.9:c.177+44905A>G ENSP00000355133.5:n.177+44905A>G
ENST00000430120.3:c.177+44905A>G ENSP00000396713.3:n.177+44905A>G
ENST00000530878.5:c.177+44905A>G ENSP00000431586.1:n.177+44905A>G
NM_001164757.1:c.177+44905A>G NP_001158229.1:n.177+44905A>G
NM_014697.2:c.177+44905A>G NP_055512.1:n.177+44905A>G
NM_014697.3:c.177+44905A>G MANE Select NP_055512.1:n.177+44905A>G
NM_001164757.2:c.177+44905A>G NP_001158229.1:n.177+44905A>G