Canonical Allele Identifier: CA2697428745
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs2102045535
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162115908A>C , CM000663.2:g.162115908A>C GRCh38
NC_000001.10:g.162085698A>C , CM000663.1:g.162085698A>C GRCh37
NC_000001.9:g.160352322A>C NCBI36
NG_015979.1:g.51118A>C
NG_015979.2:g.51118A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.106-38497A>C MANE Select ENSP00000355133.5:n.106-38497A>C
ENST00000361897.9:c.106-38497A>C ENSP00000355133.5:n.106-38497A>C
ENST00000430120.3:c.106-38497A>C ENSP00000396713.3:n.106-38497A>C
ENST00000530878.5:c.106-38497A>C ENSP00000431586.1:n.106-38497A>C
NM_001164757.1:c.106-38497A>C NP_001158229.1:n.106-38497A>C
NM_014697.2:c.106-38497A>C NP_055512.1:n.106-38497A>C
XR_922217.1:n.884-2006T>G
XR_922219.1:n.713-2006T>G
XR_922221.1:n.713-9160T>G
XR_002958375.1:n.3842-2006T>G
XR_002958378.1:n.3671-2006T>G
NM_014697.3:c.106-38497A>C MANE Select NP_055512.1:n.106-38497A>C
NM_001164757.2:c.106-38497A>C NP_001158229.1:n.106-38497A>C
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