Canonical Allele Identifier: CA2066005319

Gene: NOS1

Linked Data

• dbSNP Id: rs1874579005

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117314301_117314312del , CM000674.2:g.117314301_117314312del	GRCh38
NC_000012.11:g.117752106_117752117del , CM000674.1:g.117752106_117752117del	GRCh37
NC_000012.10:g.116236489_116236500del	NCBI36
NG_011991.2:g.52469_52480del

Transcript Alleles

HGVS	Amino-acid change
ENST00000317775.11:c.726-2717_726-2706del MANE Select	ENSP00000320758.6:n.726-2717_726-2706del
ENST00000317775.10:c.726-2717_726-2706del	ENSP00000320758.6:n.726-2717_726-2706del
ENST00000338101.8:c.726-2717_726-2706del	ENSP00000337459.4:n.726-2717_726-2706del
ENST00000344089.4:c.723-2717_723-2706del	ENSP00000339862.4:n.723-2717_723-2706del
ENST00000618760.4:c.726-2717_726-2706del	ENSP00000477999.1:n.726-2717_726-2706del
NM_000620.4:c.726-2717_726-2706del	NP_000611.1:n.726-2717_726-2706del
NM_001204218.1:c.726-2717_726-2706del	NP_001191147.1:n.726-2717_726-2706del
XM_011538398.1:c.726-2717_726-2706del	XP_011536700.1:n.726-2717_726-2706del
NM_000620.5:c.726-2717_726-2706del MANE Select	NP_000611.1:n.726-2717_726-2706del
NM_001204218.2:c.726-2717_726-2706del	NP_001191147.1:n.726-2717_726-2706del