Canonical Allele Identifier: CA15741065

Gene: NOS1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117350435C>T , CM000674.2:g.117350435C>T	GRCh38
NC_000012.11:g.117788240C>T , CM000674.1:g.117788240C>T	GRCh37
NC_000012.10:g.116272623C>T	NCBI36
NG_011991.2:g.16343G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317775.11:c.-421+11077G>A MANE Select	ENSP00000320758.6:n.-421+11077G>A
ENST00000317775.10:c.-421+11077G>A	ENSP00000320758.6:n.-421+11077G>A
ENST00000477584.1:n.119-2043G>A
ENST00000549189.1:n.471-18946G>A
ENST00000618760.4:c.-421+11077G>A	ENSP00000477999.1:n.-421+11077G>A
NM_000620.4:c.-421+11077G>A	NP_000611.1:n.-421+11077G>A
NM_001204218.1:c.-421+11077G>A	NP_001191147.1:n.-421+11077G>A
XM_011538398.1:c.-421+8556G>A	XP_011536700.1:n.-421+8556G>A
NM_000620.5:c.-421+11077G>A MANE Select	NP_000611.1:n.-421+11077G>A
NM_001204218.2:c.-421+11077G>A	NP_001191147.1:n.-421+11077G>A