Canonical Allele Identifier: CA244264883

Gene: NOS1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117300571T>C , CM000674.2:g.117300571T>C	GRCh38
NC_000012.11:g.117738376T>C , CM000674.1:g.117738376T>C	GRCh37
NC_000012.10:g.116222759T>C	NCBI36
NG_011991.2:g.66207A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317775.11:c.853-10145A>G MANE Select	ENSP00000320758.6:n.853-10145A>G
ENST00000317775.10:c.853-10145A>G	ENSP00000320758.6:n.853-10145A>G
ENST00000338101.8:c.853-10145A>G	ENSP00000337459.4:n.853-10145A>G
ENST00000344089.4:c.850-10145A>G	ENSP00000339862.4:n.850-10145A>G
ENST00000618760.4:c.853-10145A>G	ENSP00000477999.1:n.853-10145A>G
NM_000620.4:c.853-10145A>G	NP_000611.1:n.853-10145A>G
NM_001204213.1:c.-157+1445A>G	NP_001191142.1:n.-157+1445A>G
NM_001204214.1:c.-157+1445A>G	NP_001191143.1:n.-157+1445A>G
NM_001204218.1:c.853-10145A>G	NP_001191147.1:n.853-10145A>G
XM_011538398.1:c.853-10145A>G	XP_011536700.1:n.853-10145A>G
NM_000620.5:c.853-10145A>G MANE Select	NP_000611.1:n.853-10145A>G
NM_001204213.2:c.-157+1445A>G	NP_001191142.1:n.-157+1445A>G
NM_001204214.2:c.-157+1445A>G	NP_001191143.1:n.-157+1445A>G
NM_001204218.2:c.853-10145A>G	NP_001191147.1:n.853-10145A>G