Canonical Allele Identifier: CA890261997
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs1399235904

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162115804G>A , CM000663.2:g.162115804G>A GRCh38
NC_000001.10:g.162085594G>A , CM000663.1:g.162085594G>A GRCh37
NC_000001.9:g.160352218G>A NCBI36
NG_015979.1:g.51014G>A
NG_015979.2:g.51014G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.106-38601G>A MANE Select ENSP00000355133.5:n.106-38601G>A
ENST00000361897.9:c.106-38601G>A ENSP00000355133.5:n.106-38601G>A
ENST00000430120.3:c.106-38601G>A ENSP00000396713.3:n.106-38601G>A
ENST00000530878.5:c.106-38601G>A ENSP00000431586.1:n.106-38601G>A
NM_001164757.1:c.106-38601G>A NP_001158229.1:n.106-38601G>A
NM_014697.2:c.106-38601G>A NP_055512.1:n.106-38601G>A
XR_922217.1:n.884-1902C>T
XR_922219.1:n.713-1902C>T
XR_922221.1:n.713-9056C>T
XR_002958375.1:n.3842-1902C>T
XR_002958378.1:n.3671-1902C>T
NM_014697.3:c.106-38601G>A MANE Select NP_055512.1:n.106-38601G>A
NM_001164757.2:c.106-38601G>A NP_001158229.1:n.106-38601G>A