Canonical Allele Identifier: CA1008480828
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs566108964

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162115965G>T , CM000663.2:g.162115965G>T GRCh38
NC_000001.10:g.162085755G>T , CM000663.1:g.162085755G>T GRCh37
NC_000001.9:g.160352379G>T NCBI36
NG_015979.1:g.51175G>T
NG_015979.2:g.51175G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.106-38440G>T MANE Select ENSP00000355133.5:n.106-38440G>T
ENST00000361897.9:c.106-38440G>T ENSP00000355133.5:n.106-38440G>T
ENST00000430120.3:c.106-38440G>T ENSP00000396713.3:n.106-38440G>T
ENST00000530878.5:c.106-38440G>T ENSP00000431586.1:n.106-38440G>T
NM_001164757.1:c.106-38440G>T NP_001158229.1:n.106-38440G>T
NM_014697.2:c.106-38440G>T NP_055512.1:n.106-38440G>T
XR_922217.1:n.884-2063C>A
XR_922219.1:n.713-2063C>A
XR_922221.1:n.713-9217C>A
XR_002958375.1:n.3842-2063C>A
XR_002958378.1:n.3671-2063C>A
NM_014697.3:c.106-38440G>T MANE Select NP_055512.1:n.106-38440G>T
NM_001164757.2:c.106-38440G>T NP_001158229.1:n.106-38440G>T