Canonical Allele Identifier: CA2066036619

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117342417T= , CM000674.2:g.117342417T=	GRCh38
NC_000012.11:g.117780222T= , CM000674.1:g.117780222T=	GRCh37
NC_000012.10:g.116264605T=	NCBI36
NG_011991.2:g.24361A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317775.11:c.-420-10928A= MANE Select	ENSP00000320758.6:n.-420-10928A=
ENST00000317775.10:c.-420-10928A=	ENSP00000320758.6:n.-420-10928A=
ENST00000549189.1:n.471-10928A=
ENST00000618760.4:c.-420-10928A=	ENSP00000477999.1:n.-420-10928A=
NM_000620.4:c.-420-10928A=	NP_000611.1:n.-420-10928A=
NM_001204218.1:c.-420-10928A=	NP_001191147.1:n.-420-10928A=
XM_011538398.1:c.-420-10928A=	XP_011536700.1:n.-420-10928A=
NM_000620.5:c.-420-10928A= MANE Select	NP_000611.1:n.-420-10928A=
NM_001204218.2:c.-420-10928A=	NP_001191147.1:n.-420-10928A=