Canonical Allele Identifier: CA2066036223

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117342120_117342121delinsTC , CM000674.2:g.117342120_117342121delinsTC	GRCh38
NC_000012.11:g.117779925_117779926delinsTC , CM000674.1:g.117779925_117779926delinsTC	GRCh37
NC_000012.10:g.116264308_116264309delinsTC	NCBI36
NG_011991.2:g.24657_24658delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317775.11:c.-420-10632_-420-10631delinsGA MANE Select	ENSP00000320758.6:n.-420-10632_-420-10631delinsGA
ENST00000317775.10:c.-420-10632_-420-10631delinsGA	ENSP00000320758.6:n.-420-10632_-420-10631delinsGA
ENST00000549189.1:n.471-10632_471-10631delinsGA
ENST00000618760.4:c.-420-10632_-420-10631delinsGA	ENSP00000477999.1:n.-420-10632_-420-10631delinsGA
NM_000620.4:c.-420-10632_-420-10631delinsGA	NP_000611.1:n.-420-10632_-420-10631delinsGA
NM_001204218.1:c.-420-10632_-420-10631delinsGA	NP_001191147.1:n.-420-10632_-420-10631delinsGA
XM_011538398.1:c.-420-10632_-420-10631delinsGA	XP_011536700.1:n.-420-10632_-420-10631delinsGA
NM_000620.5:c.-420-10632_-420-10631delinsGA MANE Select	NP_000611.1:n.-420-10632_-420-10631delinsGA
NM_001204218.2:c.-420-10632_-420-10631delinsGA	NP_001191147.1:n.-420-10632_-420-10631delinsGA