Canonical Allele Identifier: CA358650347
Community Standard Title: NM_001083619.3(GRIA2):c.2296G>A (p.Ala766Thr)
Gene: GRIA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.157361014G>A , CM000666.2:g.157361014G>A GRCh38
NC_000004.11:g.158282166G>A , CM000666.1:g.158282166G>A GRCh37
NC_000004.10:g.158501616G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001083619.3:c.2296G>A MANE Select NP_001077088.2:p.Ala766Thr
ENST00000264426.14:c.2296G>A MANE Select ENSP00000264426.9:p.Ala766Thr
NM_000826.3:c.2292-524G>A NP_000817.2:n.2292-524G>A
NM_000826.4:c.2292-524G>A NP_000817.3:n.2292-524G>A
NM_000826.6:c.2292-524G>A NP_000817.5:n.2292-524G>A
NM_001083619.1:c.2296G>A NP_001077088.1:p.Ala766Thr
NM_001083620.1:c.2151-524G>A NP_001077089.1:n.2151-524G>A
NM_001083620.3:c.2151-524G>A NP_001077089.2:n.2151-524G>A
NM_001379000.3:c.2155G>A NP_001365929.3:p.Ala719Thr
NM_001379001.3:c.2151-524G>A NP_001365930.3:n.2151-524G>A
ENST00000264426.13:c.2296G>A ENSP00000264426.9:p.Ala766Thr
ENST00000296526.11:c.2292-524G>A ENSP00000296526.7:n.2292-524G>A
ENST00000296526.12:c.2292-524G>A ENSP00000296526.7:n.2292-524G>A
ENST00000323661.10:c.*3G>A ENSP00000318144.6:n.*3G>A
ENST00000393815.6:c.2151-524G>A ENSP00000377403.2:n.2151-524G>A
ENST00000471736.5:n.4161-524G>A
ENST00000503980.1:n.315G>A
ENST00000507898.5:c.2151-524G>A ENSP00000426845.1:n.2151-524G>A
ENST00000510854.1:c.283-524G>A
ENST00000645636.1:c.2296G>A ENSP00000495569.1:p.Ala766Thr
ENST00000703717.1:c.2155G>A ENSP00000515446.1:p.Ala719Thr
ENST00000703718.1:c.2052-524G>A ENSP00000515447.1:n.2052-524G>A
ENST00000703719.1:c.1863G>A
ENST00000703750.1:c.*1056G>A ENSP00000515459.1:n.*1056G>A
ENST00000703751.1:c.2296G>A ENSP00000515460.1:p.Ala766Thr
ENST00000703752.1:c.2155G>A ENSP00000515461.1:p.Ala719Thr
ENST00000703753.1:c.*377G>A ENSP00000515462.1:n.*377G>A
ENST00000703754.1:c.2155G>A ENSP00000515463.1:p.Ala719Thr
ENST00000703755.1:c.*482-524G>A ENSP00000515464.1:n.*482-524G>A
ENST00000703756.1:c.*578-524G>A ENSP00000515465.1:n.*578-524G>A
ENST00000703758.1:n.3487G>A
ENST00000703759.1:c.2296G>A ENSP00000515467.1:p.Ala766Thr
ENST00000703760.1:c.2319-524G>A ENSP00000515468.1:n.2319-524G>A
ENST00000703761.1:c.526-2421G>A ENSP00000515469.1:n.526-2421G>A
ENST00000703762.1:n.3149G>A
ENST00000703763.1:c.1267-2421G>A ENSP00000515470.1:n.1267-2421G>A
ENST00000703765.1:c.2151-524G>A ENSP00000515472.1:n.2151-524G>A
ENST00000703766.1:c.2023G>A
ENST00000703767.1:c.1911-524G>A ENSP00000515474.1:n.1911-524G>A
ENST00000703768.1:c.1274-524G>A
ENST00000703769.1:c.1231G>A ENSP00000515476.1:p.Ala411Thr
ENST00000703770.1:n.675G>A
XM_011531892.1:c.2296G>A XP_011530194.1:p.Ala766Thr
XR_001741212.2:n.2716G>A
XR_938725.1:n.2754G>A