Canonical Allele Identifier: CA2066005243

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117314224_117314225delinsAC , CM000674.2:g.117314224_117314225delinsAC	GRCh38
NC_000012.11:g.117752029_117752030delinsAC , CM000674.1:g.117752029_117752030delinsAC	GRCh37
NC_000012.10:g.116236412_116236413delinsAC	NCBI36
NG_011991.2:g.52553_52554delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317775.11:c.726-2633_726-2632delinsGT MANE Select	ENSP00000320758.6:n.726-2633_726-2632delinsGT
ENST00000317775.10:c.726-2633_726-2632delinsGT	ENSP00000320758.6:n.726-2633_726-2632delinsGT
ENST00000338101.8:c.726-2633_726-2632delinsGT	ENSP00000337459.4:n.726-2633_726-2632delinsGT
ENST00000344089.4:c.723-2633_723-2632delinsGT	ENSP00000339862.4:n.723-2633_723-2632delinsGT
ENST00000618760.4:c.726-2633_726-2632delinsGT	ENSP00000477999.1:n.726-2633_726-2632delinsGT
NM_000620.4:c.726-2633_726-2632delinsGT	NP_000611.1:n.726-2633_726-2632delinsGT
NM_001204218.1:c.726-2633_726-2632delinsGT	NP_001191147.1:n.726-2633_726-2632delinsGT
XM_011538398.1:c.726-2633_726-2632delinsGT	XP_011536700.1:n.726-2633_726-2632delinsGT
NM_000620.5:c.726-2633_726-2632delinsGT MANE Select	NP_000611.1:n.726-2633_726-2632delinsGT
NM_001204218.2:c.726-2633_726-2632delinsGT	NP_001191147.1:n.726-2633_726-2632delinsGT