Canonical Allele Identifier: CA2066054847

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117358091A= , CM000674.2:g.117358091A=	GRCh38
NC_000012.11:g.117795896A= , CM000674.1:g.117795896A=	GRCh37
NC_000012.10:g.116280279A=	NCBI36
NG_011991.2:g.8687T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000317775.11:c.-421+3421T= MANE Select	ENSP00000320758.6:n.-421+3421T=
ENST00000317775.10:c.-421+3421T=	ENSP00000320758.6:n.-421+3421T=
ENST00000477584.1:n.118+3421T=
ENST00000549189.1:n.471-26602T=
ENST00000618760.4:c.-421+3421T=	ENSP00000477999.1:n.-421+3421T=
NM_000620.4:c.-421+3421T=	NP_000611.1:n.-421+3421T=
NM_001204218.1:c.-421+3421T=	NP_001191147.1:n.-421+3421T=
XM_011538398.1:c.-421+900T=	XP_011536700.1:n.-421+900T=
NM_000620.5:c.-421+3421T= MANE Select	NP_000611.1:n.-421+3421T=
NM_001204218.2:c.-421+3421T=	NP_001191147.1:n.-421+3421T=