Canonical Allele Identifier: CA400667488

Gene: RGS9

Linked Data

• MyVariant Identifiers: chr17:g.63193287A>T (hg19) ; chr17:g.65197169A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65197169A>T , CM000679.2:g.65197169A>T	GRCh38
NC_000017.10:g.63193287A>T , CM000679.1:g.63193287A>T	GRCh37
NC_000017.9:g.60623749A>T	NCBI36
NG_013021.1:g.64832A>T
NG_013021.2:g.64832A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262406.10:c.904A>T MANE Select	ENSP00000262406.9:p.Asn302Tyr
ENST00000635833.1:c.904A>T	ENSP00000490658.1:p.Asn302Tyr
ENST00000262406.9:c.904A>T	ENSP00000262406.9:p.Asn302Tyr
ENST00000443584.7:c.895A>T	ENSP00000405814.3:p.Asn299Tyr
ENST00000449996.7:c.895A>T	ENSP00000396329.3:p.Asn299Tyr
ENST00000577595.1:n.832A>T
ENST00000581175.5:n.912A>T
ENST00000584234.5:c.904A>T	ENSP00000463410.1:p.Asn302Tyr
NM_001081955.2:c.895A>T	NP_001075424.1:p.Asn299Tyr
NM_001165933.1:c.895A>T	NP_001159405.1:p.Asn299Tyr
NM_003835.3:c.904A>T	NP_003826.2:p.Asn302Tyr
XM_011525426.1:c.316A>T	XP_011523728.1:p.Asn106Tyr
XM_011525426.3:c.316A>T	XP_011523728.1:p.Asn106Tyr
NM_003835.4:c.904A>T MANE Select	NP_003826.2:p.Asn302Tyr
NM_001081955.3:c.895A>T	NP_001075424.1:p.Asn299Tyr
NM_001165933.2:c.895A>T	NP_001159405.1:p.Asn299Tyr