Canonical Allele Identifier: CA12733844

Gene: RGS22

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.100012277A>C , CM000670.2:g.100012277A>C	GRCh38
NC_000008.10:g.101024505A>C , CM000670.1:g.101024505A>C	GRCh37
NC_000008.9:g.101093681A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360863.11:c.2167-3708T>G MANE Select	ENSP00000354109.6:n.2167-3708T>G
ENST00000360863.10:c.2167-3708T>G	ENSP00000354109.6:n.2167-3708T>G
ENST00000517769.5:n.395-3708T>G
ENST00000517828.5:c.112-3708T>G	ENSP00000427754.1:n.112-3708T>G
ENST00000519725.5:c.*742-3708T>G	ENSP00000427798.1:n.*742-3708T>G
ENST00000523287.5:c.1624-3708T>G	ENSP00000429382.1:n.1624-3708T>G
ENST00000523437.5:c.2131-3708T>G	ENSP00000428212.1:n.2131-3708T>G
ENST00000617334.1:c.2131-3708T>G	ENSP00000479205.1:n.2131-3708T>G
NM_001286692.1:c.2131-3708T>G	NP_001273621.1:n.2131-3708T>G
NM_001286693.1:c.1624-3708T>G	NP_001273622.1:n.1624-3708T>G
NM_015668.4:c.2167-3708T>G	NP_056483.3:n.2167-3708T>G
XM_005250856.2:c.2167-3708T>G	XP_005250913.1:n.2167-3708T>G
XM_005250857.2:c.2167-3708T>G	XP_005250914.1:n.2167-3708T>G
XM_005250858.2:c.2167-3708T>G	XP_005250915.1:n.2167-3708T>G
XM_005250860.2:c.2167-3708T>G	XP_005250917.1:n.2167-3708T>G
XM_006716540.2:c.1879-3708T>G	XP_006716603.1:n.1879-3708T>G
XM_011516957.1:c.1879-3708T>G	XP_011515259.1:n.1879-3708T>G
XM_011516958.1:c.1879-3708T>G	XP_011515260.1:n.1879-3708T>G
XM_011516959.1:c.*4-3708T>G	XP_011515261.1:n.*4-3708T>G
XR_928317.1:n.1865-3708T>G
XM_005250856.3:c.2167-3708T>G	XP_005250913.1:n.2167-3708T>G
XM_005250857.3:c.2167-3708T>G	XP_005250914.1:n.2167-3708T>G
XM_005250858.3:c.2167-3708T>G	XP_005250915.1:n.2167-3708T>G
XM_005250860.3:c.2167-3708T>G	XP_005250917.1:n.2167-3708T>G
XM_011516959.3:c.*4-3708T>G	XP_011515261.1:n.*4-3708T>G
XM_017013309.2:c.2167-3708T>G	XP_016868798.1:n.2167-3708T>G
XM_017013310.2:c.2167-3708T>G	XP_016868799.1:n.2167-3708T>G
XM_017013311.1:c.802-3708T>G	XP_016868800.1:n.802-3708T>G
XM_024447121.1:c.334-3708T>G	XP_024302889.1:n.334-3708T>G
XM_024447122.1:c.334-3708T>G	XP_024302890.1:n.334-3708T>G
NM_015668.5:c.2167-3708T>G MANE Select	NP_056483.3:n.2167-3708T>G
NM_001286692.2:c.2131-3708T>G	NP_001273621.1:n.2131-3708T>G
NM_001286693.2:c.1624-3708T>G	NP_001273622.1:n.1624-3708T>G