Canonical Allele Identifier: CA10817084
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs4657175

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162225948T>G , CM000663.2:g.162225948T>G GRCh38
NC_000001.10:g.162195738T>G , CM000663.1:g.162195738T>G GRCh37
NC_000001.9:g.160462362T>G NCBI36
NG_015979.1:g.161158T>G
NG_015979.2:g.161158T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.178-61396T>G MANE Select ENSP00000355133.5:n.178-61396T>G
ENST00000361897.9:c.178-61396T>G ENSP00000355133.5:n.178-61396T>G
ENST00000430120.3:c.178-61396T>G ENSP00000396713.3:n.178-61396T>G
ENST00000530878.5:c.178-61396T>G ENSP00000431586.1:n.178-61396T>G
NM_001164757.1:c.178-61396T>G NP_001158229.1:n.178-61396T>G
NM_014697.2:c.178-61396T>G NP_055512.1:n.178-61396T>G
NM_014697.3:c.178-61396T>G MANE Select NP_055512.1:n.178-61396T>G
NM_001164757.2:c.178-61396T>G NP_001158229.1:n.178-61396T>G