Canonical Allele Identifier: CA31618911
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs916973358

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162115974T>C , CM000663.2:g.162115974T>C GRCh38
NC_000001.10:g.162085764T>C , CM000663.1:g.162085764T>C GRCh37
NC_000001.9:g.160352388T>C NCBI36
NG_015979.1:g.51184T>C
NG_015979.2:g.51184T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.106-38431T>C MANE Select ENSP00000355133.5:n.106-38431T>C
ENST00000361897.9:c.106-38431T>C ENSP00000355133.5:n.106-38431T>C
ENST00000430120.3:c.106-38431T>C ENSP00000396713.3:n.106-38431T>C
ENST00000530878.5:c.106-38431T>C ENSP00000431586.1:n.106-38431T>C
NM_001164757.1:c.106-38431T>C NP_001158229.1:n.106-38431T>C
NM_014697.2:c.106-38431T>C NP_055512.1:n.106-38431T>C
XR_922217.1:n.884-2072A>G
XR_922219.1:n.713-2072A>G
XR_922221.1:n.713-9226A>G
XR_002958375.1:n.3842-2072A>G
XR_002958378.1:n.3671-2072A>G
NM_014697.3:c.106-38431T>C MANE Select NP_055512.1:n.106-38431T>C
NM_001164757.2:c.106-38431T>C NP_001158229.1:n.106-38431T>C