Canonical Allele Identifier: CA2797626082

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117307109A>T , CM000674.2:g.117307109A>T	GRCh38
NC_000012.11:g.117744914A>T , CM000674.1:g.117744914A>T	GRCh37
NC_000012.10:g.116229297A>T	NCBI36
NG_011991.2:g.59669T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317775.11:c.852+4357T>A MANE Select	ENSP00000320758.6:n.852+4357T>A
ENST00000317775.10:c.852+4357T>A	ENSP00000320758.6:n.852+4357T>A
ENST00000338101.8:c.852+4357T>A	ENSP00000337459.4:n.852+4357T>A
ENST00000344089.4:c.849+4357T>A	ENSP00000339862.4:n.849+4357T>A
ENST00000618760.4:c.852+4357T>A	ENSP00000477999.1:n.852+4357T>A
NM_000620.4:c.852+4357T>A	NP_000611.1:n.852+4357T>A
NM_001204214.1:c.-213+2208T>A	NP_001191143.1:n.-213+2208T>A
NM_001204218.1:c.852+4357T>A	NP_001191147.1:n.852+4357T>A
XM_011538398.1:c.852+4357T>A	XP_011536700.1:n.852+4357T>A
NM_000620.5:c.852+4357T>A MANE Select	NP_000611.1:n.852+4357T>A
NM_001204214.2:c.-213+2208T>A	NP_001191143.1:n.-213+2208T>A
NM_001204218.2:c.852+4357T>A	NP_001191147.1:n.852+4357T>A