Canonical Allele Identifier: CA1203049819
Gene: NOS1AP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162199592T= , CM000663.2:g.162199592T= GRCh38
NC_000001.10:g.162169382T= , CM000663.1:g.162169382T= GRCh37
NC_000001.9:g.160436006T= NCBI36
NG_015979.1:g.134802T=
NG_015979.2:g.134802T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361897.10:c.177+45116T= MANE Select ENSP00000355133.5:n.177+45116T=
ENST00000361897.9:c.177+45116T= ENSP00000355133.5:n.177+45116T=
ENST00000430120.3:c.177+45116T= ENSP00000396713.3:n.177+45116T=
ENST00000530878.5:c.177+45116T= ENSP00000431586.1:n.177+45116T=
NM_001164757.1:c.177+45116T= NP_001158229.1:n.177+45116T=
NM_014697.2:c.177+45116T= NP_055512.1:n.177+45116T=
NM_014697.3:c.177+45116T= MANE Select NP_055512.1:n.177+45116T=
NM_001164757.2:c.177+45116T= NP_001158229.1:n.177+45116T=
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