Canonical Allele Identifier: CA2270723667

Gene: RGS9

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65198827A= , CM000679.2:g.65198827A=	GRCh38
NC_000017.10:g.63194945A= , CM000679.1:g.63194945A=	GRCh37
NC_000017.9:g.60625407A=	NCBI36
NG_013021.1:g.66490A=
NG_013021.2:g.66490A=

Transcript Alleles

HGVS	Amino-acid Change
NM_003835.4:c.976+1586A= MANE Select	NP_003826.2:n.976+1586A=
ENST00000262406.10:c.976+1586A= MANE Select	ENSP00000262406.9:n.976+1586A=
NM_001081955.2:c.967+1586A=	NP_001075424.1:n.967+1586A=
NM_001081955.3:c.967+1586A=	NP_001075424.1:n.967+1586A=
NM_001165933.1:c.967+1586A=	NP_001159405.1:n.967+1586A=
NM_001165933.2:c.967+1586A=	NP_001159405.1:n.967+1586A=
NM_003835.3:c.976+1586A=	NP_003826.2:n.976+1586A=
ENST00000262406.9:c.976+1586A=	ENSP00000262406.9:n.976+1586A=
ENST00000443584.7:c.967+1586A=	ENSP00000405814.3:n.967+1586A=
ENST00000449996.7:c.967+1586A=	ENSP00000396329.3:n.967+1586A=
ENST00000577595.1:n.904+1586A=
ENST00000581175.5:n.984+1586A=
ENST00000584234.5:c.976+1586A=	ENSP00000463410.1:n.976+1586A=
ENST00000635833.1:c.976+1586A=	ENSP00000490658.1:n.976+1586A=
XM_011525426.1:c.388+1586A=	XP_011523728.1:n.388+1586A=
XM_011525426.3:c.388+1586A=	XP_011523728.1:n.388+1586A=