Canonical Allele Identifier: CA400667432

Gene: RGS9

Linked Data

• MyVariant Identifiers: chr17:g.63193279G>A (hg19) ; chr17:g.65197161G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65197161G>A , CM000679.2:g.65197161G>A	GRCh38
NC_000017.10:g.63193279G>A , CM000679.1:g.63193279G>A	GRCh37
NC_000017.9:g.60623741G>A	NCBI36
NG_013021.1:g.64824G>A
NG_013021.2:g.64824G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262406.10:c.896G>A MANE Select	ENSP00000262406.9:p.Trp299Ter
ENST00000635833.1:c.896G>A	ENSP00000490658.1:p.Trp299Ter
ENST00000262406.9:c.896G>A	ENSP00000262406.9:p.Trp299Ter
ENST00000443584.7:c.887G>A	ENSP00000405814.3:p.Trp296Ter
ENST00000449996.7:c.887G>A	ENSP00000396329.3:p.Trp296Ter
ENST00000577595.1:n.824G>A
ENST00000581175.5:n.904G>A
ENST00000584234.5:c.896G>A	ENSP00000463410.1:p.Trp299Ter
NM_001081955.2:c.887G>A	NP_001075424.1:p.Trp296Ter
NM_001165933.1:c.887G>A	NP_001159405.1:p.Trp296Ter
NM_003835.3:c.896G>A	NP_003826.2:p.Trp299Ter
XM_011525426.1:c.308G>A	XP_011523728.1:p.Trp103Ter
XM_011525426.3:c.308G>A	XP_011523728.1:p.Trp103Ter
NM_003835.4:c.896G>A MANE Select	NP_003826.2:p.Trp299Ter
NM_001081955.3:c.887G>A	NP_001075424.1:p.Trp296Ter
NM_001165933.2:c.887G>A	NP_001159405.1:p.Trp296Ter