Canonical Allele Identifier: CA890262004

Gene: NOS1AP

Linked Data

• dbSNP Id: rs1197318480
• MyVariant Identifiers: chr1:g.162085730C>G (hg19) ; chr1:g.162115940C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162115940C>G , CM000663.2:g.162115940C>G	GRCh38
NC_000001.10:g.162085730C>G , CM000663.1:g.162085730C>G	GRCh37
NC_000001.9:g.160352354C>G	NCBI36
NG_015979.1:g.51150C>G
NG_015979.2:g.51150C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361897.10:c.106-38465C>G MANE Select	ENSP00000355133.5:n.106-38465C>G
ENST00000361897.9:c.106-38465C>G	ENSP00000355133.5:n.106-38465C>G
ENST00000430120.3:c.106-38465C>G	ENSP00000396713.3:n.106-38465C>G
ENST00000530878.5:c.106-38465C>G	ENSP00000431586.1:n.106-38465C>G
NM_001164757.1:c.106-38465C>G	NP_001158229.1:n.106-38465C>G
NM_014697.2:c.106-38465C>G	NP_055512.1:n.106-38465C>G
XR_922217.1:n.884-2038G>C
XR_922219.1:n.713-2038G>C
XR_922221.1:n.713-9192G>C
XR_002958375.1:n.3842-2038G>C
XR_002958378.1:n.3671-2038G>C
NM_014697.3:c.106-38465C>G MANE Select	NP_055512.1:n.106-38465C>G
NM_001164757.2:c.106-38465C>G	NP_001158229.1:n.106-38465C>G