Canonical Allele Identifier: CA2270735899

Gene: RGS9

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65225096G= , CM000679.2:g.65225096G=	GRCh38
NC_000017.10:g.63221214G= , CM000679.1:g.63221214G=	GRCh37
NC_000017.9:g.60651676G=	NCBI36
NG_013021.1:g.92759G=
NG_013021.2:g.92759G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003835.4:c.1502G= MANE Select	NP_003826.2:p.Arg501=
ENST00000262406.10:c.1502G= MANE Select	ENSP00000262406.9:p.Arg501=
NM_001081955.2:c.1493G=	NP_001075424.1:p.Arg498=
NM_001081955.3:c.1493G=	NP_001075424.1:p.Arg498=
NM_003835.3:c.1502G=	NP_003826.2:p.Arg501=
ENST00000262406.9:c.1502G=	ENSP00000262406.9:p.Arg501=
ENST00000443584.7:c.1493G=	ENSP00000405814.3:p.Arg498=
ENST00000449996.7:c.1493G=	ENSP00000396329.3:p.Arg498=
ENST00000577595.1:n.1430G=
ENST00000584234.5:c.*21G=	ENSP00000463410.1:n.*21G=
ENST00000635833.1:c.1502G=	ENSP00000490658.1:p.Arg501=
XM_011525426.1:c.914G=	XP_011523728.1:p.Arg305=
XM_011525426.3:c.914G=	XP_011523728.1:p.Arg305=