Canonical Allele Identifier: CA2065984951

Gene: NOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117292535G= , CM000674.2:g.117292535G=	GRCh38
NC_000012.11:g.117730340G= , CM000674.1:g.117730340G=	GRCh37
NC_000012.10:g.116214723G=	NCBI36
NG_011991.2:g.74243C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000620.5:c.853-2109C= MANE Select	NP_000611.1:n.853-2109C=
ENST00000317775.11:c.853-2109C= MANE Select	ENSP00000320758.6:n.853-2109C=
NM_000620.4:c.853-2109C=	NP_000611.1:n.853-2109C=
NM_001204213.1:c.-156-2109C=	NP_001191142.1:n.-156-2109C=
NM_001204213.2:c.-156-2109C=	NP_001191142.1:n.-156-2109C=
NM_001204214.1:c.-156-2109C=	NP_001191143.1:n.-156-2109C=
NM_001204214.2:c.-156-2109C=	NP_001191143.1:n.-156-2109C=
NM_001204218.1:c.853-2109C=	NP_001191147.1:n.853-2109C=
NM_001204218.2:c.853-2109C=	NP_001191147.1:n.853-2109C=
ENST00000317775.10:c.853-2109C=	ENSP00000320758.6:n.853-2109C=
ENST00000338101.8:c.853-2109C=	ENSP00000337459.4:n.853-2109C=
ENST00000344089.4:c.850-2109C=	ENSP00000339862.4:n.850-2109C=
ENST00000618760.4:c.853-2109C=	ENSP00000477999.1:n.853-2109C=
XM_011538398.1:c.853-2109C=	XP_011536700.1:n.853-2109C=