Canonical Allele Identifier: CA2270722940

Gene: RGS9

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65197167T= , CM000679.2:g.65197167T=	GRCh38
NC_000017.10:g.63193285T= , CM000679.1:g.63193285T=	GRCh37
NC_000017.9:g.60623747T=	NCBI36
NG_013021.1:g.64830T=
NG_013021.2:g.64830T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262406.10:c.902T= MANE Select	ENSP00000262406.9:p.Phe301=
ENST00000635833.1:c.902T=	ENSP00000490658.1:p.Phe301=
ENST00000262406.9:c.902T=	ENSP00000262406.9:p.Phe301=
ENST00000443584.7:c.893T=	ENSP00000405814.3:p.Phe298=
ENST00000449996.7:c.893T=	ENSP00000396329.3:p.Phe298=
ENST00000577595.1:n.830T=
ENST00000581175.5:n.910T=
ENST00000584234.5:c.902T=	ENSP00000463410.1:p.Phe301=
NM_001081955.2:c.893T=	NP_001075424.1:p.Phe298=
NM_001165933.1:c.893T=	NP_001159405.1:p.Phe298=
NM_003835.3:c.902T=	NP_003826.2:p.Phe301=
XM_011525426.1:c.314T=	XP_011523728.1:p.Phe105=
XM_011525426.3:c.314T=	XP_011523728.1:p.Phe105=
NM_003835.4:c.902T= MANE Select	NP_003826.2:p.Phe301=
NM_001081955.3:c.893T=	NP_001075424.1:p.Phe298=
NM_001165933.2:c.893T=	NP_001159405.1:p.Phe298=