Canonical Allele Identifier: CA2066054877

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117358121T= , CM000674.2:g.117358121T=	GRCh38
NC_000012.11:g.117795926T= , CM000674.1:g.117795926T=	GRCh37
NC_000012.10:g.116280309T=	NCBI36
NG_011991.2:g.8657A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000317775.11:c.-421+3391A= MANE Select	ENSP00000320758.6:n.-421+3391A=
ENST00000317775.10:c.-421+3391A=	ENSP00000320758.6:n.-421+3391A=
ENST00000477584.1:n.118+3391A=
ENST00000549189.1:n.471-26632A=
ENST00000618760.4:c.-421+3391A=	ENSP00000477999.1:n.-421+3391A=
NM_000620.4:c.-421+3391A=	NP_000611.1:n.-421+3391A=
NM_001204218.1:c.-421+3391A=	NP_001191147.1:n.-421+3391A=
XM_011538398.1:c.-421+870A=	XP_011536700.1:n.-421+870A=
NM_000620.5:c.-421+3391A= MANE Select	NP_000611.1:n.-421+3391A=
NM_001204218.2:c.-421+3391A=	NP_001191147.1:n.-421+3391A=