Canonical Allele Identifier: CA2797626253

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117313524_117313527del , CM000674.2:g.117313524_117313527del	GRCh38
NC_000012.11:g.117751329_117751332del , CM000674.1:g.117751329_117751332del	GRCh37
NC_000012.10:g.116235712_116235715del	NCBI36
NG_011991.2:g.53252_53255del

Transcript Alleles

HGVS	Amino-acid change
ENST00000317775.11:c.726-1934_726-1931del MANE Select	ENSP00000320758.6:n.726-1934_726-1931del
ENST00000317775.10:c.726-1934_726-1931del	ENSP00000320758.6:n.726-1934_726-1931del
ENST00000338101.8:c.726-1934_726-1931del	ENSP00000337459.4:n.726-1934_726-1931del
ENST00000344089.4:c.723-1934_723-1931del	ENSP00000339862.4:n.723-1934_723-1931del
ENST00000618760.4:c.726-1934_726-1931del	ENSP00000477999.1:n.726-1934_726-1931del
NM_000620.4:c.726-1934_726-1931del	NP_000611.1:n.726-1934_726-1931del
NM_001204218.1:c.726-1934_726-1931del	NP_001191147.1:n.726-1934_726-1931del
XM_011538398.1:c.726-1934_726-1931del	XP_011536700.1:n.726-1934_726-1931del
NM_000620.5:c.726-1934_726-1931del MANE Select	NP_000611.1:n.726-1934_726-1931del
NM_001204218.2:c.726-1934_726-1931del	NP_001191147.1:n.726-1934_726-1931del