Canonical Allele Identifier: CA2697370203

Gene: NOS1AP

Linked Data

• dbSNP Id: rs2101813383

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162349773C>G , CM000663.2:g.162349773C>G	GRCh38
NC_000001.10:g.162319563C>G , CM000663.1:g.162319563C>G	GRCh37
NC_000001.9:g.160586187C>G	NCBI36
NG_015979.1:g.284983C>G
NG_015979.2:g.284983C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361897.10:c.596-5414C>G MANE Select	ENSP00000355133.5:n.596-5414C>G
ENST00000361897.9:c.596-5414C>G	ENSP00000355133.5:n.596-5414C>G
ENST00000430120.3:c.581-5414C>G	ENSP00000396713.3:n.581-5414C>G
ENST00000530878.5:c.581-5414C>G	ENSP00000431586.1:n.581-5414C>G
NM_001164757.1:c.581-5414C>G	NP_001158229.1:n.581-5414C>G
NM_014697.2:c.596-5414C>G	NP_055512.1:n.596-5414C>G
NM_014697.3:c.596-5414C>G MANE Select	NP_055512.1:n.596-5414C>G
NM_001164757.2:c.581-5414C>G	NP_001158229.1:n.581-5414C>G