Canonical Allele Identifier: CA1203017007
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs1571023893

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162115737T>G , CM000663.2:g.162115737T>G GRCh38
NC_000001.10:g.162085527T>G , CM000663.1:g.162085527T>G GRCh37
NC_000001.9:g.160352151T>G NCBI36
NG_015979.1:g.50947T>G
NG_015979.2:g.50947T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.106-38668T>G MANE Select ENSP00000355133.5:n.106-38668T>G
ENST00000361897.9:c.106-38668T>G ENSP00000355133.5:n.106-38668T>G
ENST00000430120.3:c.106-38668T>G ENSP00000396713.3:n.106-38668T>G
ENST00000530878.5:c.106-38668T>G ENSP00000431586.1:n.106-38668T>G
NM_001164757.1:c.106-38668T>G NP_001158229.1:n.106-38668T>G
NM_014697.2:c.106-38668T>G NP_055512.1:n.106-38668T>G
XR_922217.1:n.884-1835A>C
XR_922219.1:n.713-1835A>C
XR_922221.1:n.713-8989A>C
XR_002958375.1:n.3842-1835A>C
XR_002958378.1:n.3671-1835A>C
NM_014697.3:c.106-38668T>G MANE Select NP_055512.1:n.106-38668T>G
NM_001164757.2:c.106-38668T>G NP_001158229.1:n.106-38668T>G