Canonical Allele Identifier: CA15084007
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs12734991

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162224786C>T , CM000663.2:g.162224786C>T GRCh38
NC_000001.10:g.162194576C>T , CM000663.1:g.162194576C>T GRCh37
NC_000001.9:g.160461200C>T NCBI36
NG_015979.1:g.159996C>T
NG_015979.2:g.159996C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.178-62558C>T MANE Select ENSP00000355133.5:n.178-62558C>T
ENST00000361897.9:c.178-62558C>T ENSP00000355133.5:n.178-62558C>T
ENST00000430120.3:c.178-62558C>T ENSP00000396713.3:n.178-62558C>T
ENST00000530878.5:c.178-62558C>T ENSP00000431586.1:n.178-62558C>T
NM_001164757.1:c.178-62558C>T NP_001158229.1:n.178-62558C>T
NM_014697.2:c.178-62558C>T NP_055512.1:n.178-62558C>T
NM_014697.3:c.178-62558C>T MANE Select NP_055512.1:n.178-62558C>T
NM_001164757.2:c.178-62558C>T NP_001158229.1:n.178-62558C>T