Canonical Allele Identifier: CA2270725129

Gene: RGS9

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65201814C= , CM000679.2:g.65201814C=	GRCh38
NC_000017.10:g.63197932C= , CM000679.1:g.63197932C=	GRCh37
NC_000017.9:g.60628394C=	NCBI36
NG_013021.1:g.69477C=
NG_013021.2:g.69477C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262406.10:c.977-179C= MANE Select	ENSP00000262406.9:n.977-179C=
ENST00000635833.1:c.977-179C=	ENSP00000490658.1:n.977-179C=
ENST00000262406.9:c.977-179C=	ENSP00000262406.9:n.977-179C=
ENST00000443584.7:c.968-179C=	ENSP00000405814.3:n.968-179C=
ENST00000449996.7:c.968-179C=	ENSP00000396329.3:n.968-179C=
ENST00000577595.1:n.905-179C=
ENST00000581175.5:n.985-179C=
ENST00000584234.5:c.977-179C=	ENSP00000463410.1:n.977-179C=
NM_001081955.2:c.968-179C=	NP_001075424.1:n.968-179C=
NM_001165933.1:c.968-179C=	NP_001159405.1:n.968-179C=
NM_003835.3:c.977-179C=	NP_003826.2:n.977-179C=
XM_011525426.1:c.389-179C=	XP_011523728.1:n.389-179C=
XM_011525426.3:c.389-179C=	XP_011523728.1:n.389-179C=
NM_003835.4:c.977-179C= MANE Select	NP_003826.2:n.977-179C=
NM_001081955.3:c.968-179C=	NP_001075424.1:n.968-179C=
NM_001165933.2:c.968-179C=	NP_001159405.1:n.968-179C=