Canonical Allele Identifier: CA13778699

Gene: NOS1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117232493C>G , CM000674.2:g.117232493C>G	GRCh38
NC_000012.11:g.117670298C>G , CM000674.1:g.117670298C>G	GRCh37
NC_000012.10:g.116154681C>G	NCBI36
NG_011991.2:g.134285G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317775.11:c.3236-362G>C MANE Select	ENSP00000320758.6:n.3236-362G>C
ENST00000317775.10:c.3236-362G>C	ENSP00000320758.6:n.3236-362G>C
ENST00000338101.8:c.3338-362G>C	ENSP00000337459.4:n.3338-362G>C
ENST00000344089.4:c.3233-362G>C	ENSP00000339862.4:n.3233-362G>C
ENST00000618760.4:c.3338-362G>C	ENSP00000477999.1:n.3338-362G>C
NM_000620.4:c.3236-362G>C	NP_000611.1:n.3236-362G>C
NM_001204213.1:c.2228-362G>C	NP_001191142.1:n.2228-362G>C
NM_001204214.1:c.2228-362G>C	NP_001191143.1:n.2228-362G>C
NM_001204218.1:c.3338-362G>C	NP_001191147.1:n.3338-362G>C
XM_011538398.1:c.3338-362G>C	XP_011536700.1:n.3338-362G>C
NM_000620.5:c.3236-362G>C MANE Select	NP_000611.1:n.3236-362G>C
NM_001204213.2:c.2228-362G>C	NP_001191142.1:n.2228-362G>C
NM_001204214.2:c.2228-362G>C	NP_001191143.1:n.2228-362G>C
NM_001204218.2:c.3338-362G>C	NP_001191147.1:n.3338-362G>C