Canonical Allele Identifier: CA14424006

Gene: RGS9

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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