Canonical Allele Identifier: CA2066046757

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117350435C= , CM000674.2:g.117350435C=	GRCh38
NC_000012.11:g.117788240C= , CM000674.1:g.117788240C=	GRCh37
NC_000012.10:g.116272623C=	NCBI36
NG_011991.2:g.16343G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000620.5:c.-421+11077G= MANE Select	NP_000611.1:n.-421+11077G=
ENST00000317775.11:c.-421+11077G= MANE Select	ENSP00000320758.6:n.-421+11077G=
NM_000620.4:c.-421+11077G=	NP_000611.1:n.-421+11077G=
NM_001204218.1:c.-421+11077G=	NP_001191147.1:n.-421+11077G=
NM_001204218.2:c.-421+11077G=	NP_001191147.1:n.-421+11077G=
ENST00000317775.10:c.-421+11077G=	ENSP00000320758.6:n.-421+11077G=
ENST00000477584.1:n.119-2043G=
ENST00000549189.1:n.471-18946G=
ENST00000618760.4:c.-421+11077G=	ENSP00000477999.1:n.-421+11077G=
XM_011538398.1:c.-421+8556G=	XP_011536700.1:n.-421+8556G=