Canonical Allele Identifier: CA2270719914

Gene: RGS9

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65190194C= , CM000679.2:g.65190194C=	GRCh38
NC_000017.10:g.63186312C= , CM000679.1:g.63186312C=	GRCh37
NC_000017.9:g.60616774C=	NCBI36
NG_013021.1:g.57857C=
NG_013021.2:g.57857C=

Transcript Alleles

HGVS	Amino-acid Change
NM_003835.4:c.704C= MANE Select	NP_003826.2:p.Ala235=
ENST00000262406.10:c.704C= MANE Select	ENSP00000262406.9:p.Ala235=
NM_001081955.2:c.695C=	NP_001075424.1:p.Ala232=
NM_001081955.3:c.695C=	NP_001075424.1:p.Ala232=
NM_001165933.1:c.695C=	NP_001159405.1:p.Ala232=
NM_001165933.2:c.695C=	NP_001159405.1:p.Ala232=
NM_003835.3:c.704C=	NP_003826.2:p.Ala235=
ENST00000262406.9:c.704C=	ENSP00000262406.9:p.Ala235=
ENST00000443584.7:c.695C=	ENSP00000405814.3:p.Ala232=
ENST00000449996.7:c.695C=	ENSP00000396329.3:p.Ala232=
ENST00000577595.1:n.632C=
ENST00000581175.5:n.712C=
ENST00000584234.5:c.704C=	ENSP00000463410.1:p.Ala235=
ENST00000635833.1:c.704C=	ENSP00000490658.1:p.Ala235=
XM_011525426.1:c.116C=	XP_011523728.1:p.Ala39=
XM_011525426.3:c.116C=	XP_011523728.1:p.Ala39=