Canonical Allele Identifier: CA358648413

Gene: GRIA2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.157336613C>A , CM000666.2:g.157336613C>A	GRCh38
NC_000004.11:g.158257765C>A , CM000666.1:g.158257765C>A	GRCh37
NC_000004.10:g.158477215C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001083619.3:c.1710C>A MANE Select	NP_001077088.2:p.Tyr570Ter
ENST00000264426.14:c.1710C>A MANE Select	ENSP00000264426.9:p.Tyr570Ter
NM_000826.3:c.1710C>A	NP_000817.2:p.Tyr570Ter
NM_000826.4:c.1710C>A	NP_000817.3:p.Tyr570Ter
NM_000826.6:c.1710C>A	NP_000817.5:p.Tyr570Ter
NM_001083619.1:c.1710C>A	NP_001077088.1:p.Tyr570Ter
NM_001083620.1:c.1569C>A	NP_001077089.1:p.Tyr523Ter
NM_001083620.3:c.1569C>A	NP_001077089.2:p.Tyr523Ter
NM_001379000.3:c.1569C>A	NP_001365929.3:p.Tyr523Ter
NM_001379001.3:c.1569C>A	NP_001365930.3:p.Tyr523Ter
ENST00000264426.13:c.1710C>A	ENSP00000264426.9:p.Tyr570Ter
ENST00000296526.11:c.1710C>A	ENSP00000296526.7:p.Tyr570Ter
ENST00000296526.12:c.1710C>A	ENSP00000296526.7:p.Tyr570Ter
ENST00000323661.10:c.1569C>A	ENSP00000318144.6:p.Tyr523Ter
ENST00000393815.6:c.1569C>A	ENSP00000377403.2:p.Tyr523Ter
ENST00000471736.5:n.3579C>A
ENST00000507898.5:c.1569C>A	ENSP00000426845.1:p.Tyr523Ter
ENST00000645636.1:c.1710C>A	ENSP00000495569.1:p.Tyr570Ter
ENST00000703717.1:c.1569C>A	ENSP00000515446.1:p.Tyr523Ter
ENST00000703718.1:c.1470C>A	ENSP00000515447.1:p.Tyr490Ter
ENST00000703719.1:c.1277C>A
ENST00000703750.1:c.*394-172C>A	ENSP00000515459.1:n.*394-172C>A
ENST00000703751.1:c.1710C>A	ENSP00000515460.1:p.Tyr570Ter
ENST00000703752.1:c.1569C>A	ENSP00000515461.1:p.Tyr523Ter
ENST00000703753.1:c.1668+42C>A	ENSP00000515462.1:n.1668+42C>A
ENST00000703754.1:c.1569C>A	ENSP00000515463.1:p.Tyr523Ter
ENST00000703755.1:c.*34+268C>A	ENSP00000515464.1:n.*34+268C>A
ENST00000703756.1:c.1470C>A	ENSP00000515465.1:p.Tyr490Ter
ENST00000703758.1:n.2035C>A
ENST00000703759.1:c.1710C>A	ENSP00000515467.1:p.Tyr570Ter
ENST00000703760.1:c.1737C>A	ENSP00000515468.1:p.Tyr579Ter
ENST00000703761.1:c.525+23738C>A	ENSP00000515469.1:n.525+23738C>A
ENST00000703762.1:n.2522C>A
ENST00000703763.1:c.1266+2493C>A	ENSP00000515470.1:n.1266+2493C>A
ENST00000703765.1:c.1569C>A	ENSP00000515472.1:p.Tyr523Ter
ENST00000703766.1:c.1320-172C>A
ENST00000703767.1:c.1329C>A	ENSP00000515474.1:p.Tyr443Ter
ENST00000703768.1:c.692C>A
ENST00000703769.1:c.645C>A	ENSP00000515476.1:p.Tyr215Ter
ENST00000703770.1:n.223+42C>A
XM_011531892.1:c.1710C>A	XP_011530194.1:p.Tyr570Ter
XR_001741212.2:n.2130C>A
XR_938725.1:n.2168C>A