Canonical Allele Identifier: CA526974366
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs1334832571

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162115876A>G , CM000663.2:g.162115876A>G GRCh38
NC_000001.10:g.162085666A>G , CM000663.1:g.162085666A>G GRCh37
NC_000001.9:g.160352290A>G NCBI36
NG_015979.1:g.51086A>G
NG_015979.2:g.51086A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.106-38529A>G MANE Select ENSP00000355133.5:n.106-38529A>G
ENST00000361897.9:c.106-38529A>G ENSP00000355133.5:n.106-38529A>G
ENST00000430120.3:c.106-38529A>G ENSP00000396713.3:n.106-38529A>G
ENST00000530878.5:c.106-38529A>G ENSP00000431586.1:n.106-38529A>G
NM_001164757.1:c.106-38529A>G NP_001158229.1:n.106-38529A>G
NM_014697.2:c.106-38529A>G NP_055512.1:n.106-38529A>G
XR_922217.1:n.884-1974T>C
XR_922219.1:n.713-1974T>C
XR_922221.1:n.713-9128T>C
XR_002958375.1:n.3842-1974T>C
XR_002958378.1:n.3671-1974T>C
NM_014697.3:c.106-38529A>G MANE Select NP_055512.1:n.106-38529A>G
NM_001164757.2:c.106-38529A>G NP_001158229.1:n.106-38529A>G