Canonical Allele Identifier: CA2066004431

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117281017C= , CM000674.2:g.117281017C=	GRCh38
NC_000012.11:g.117718822C= , CM000674.1:g.117718822C=	GRCh37
NC_000012.10:g.116203205C=	NCBI36
NG_011991.2:g.85761G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000620.5:c.1383-151G= MANE Select	NP_000611.1:n.1383-151G=
ENST00000317775.11:c.1383-151G= MANE Select	ENSP00000320758.6:n.1383-151G=
NM_000620.4:c.1383-151G=	NP_000611.1:n.1383-151G=
NM_001204213.1:c.375-151G=	NP_001191142.1:n.375-151G=
NM_001204213.2:c.375-151G=	NP_001191142.1:n.375-151G=
NM_001204214.1:c.375-151G=	NP_001191143.1:n.375-151G=
NM_001204214.2:c.375-151G=	NP_001191143.1:n.375-151G=
NM_001204218.1:c.1383-151G=	NP_001191147.1:n.1383-151G=
NM_001204218.2:c.1383-151G=	NP_001191147.1:n.1383-151G=
ENST00000317775.10:c.1383-151G=	ENSP00000320758.6:n.1383-151G=
ENST00000338101.8:c.1383-151G=	ENSP00000337459.4:n.1383-151G=
ENST00000344089.4:c.1380-151G=	ENSP00000339862.4:n.1380-151G=
ENST00000618760.4:c.1383-151G=	ENSP00000477999.1:n.1383-151G=
XM_011538398.1:c.1383-151G=	XP_011536700.1:n.1383-151G=