Canonical Allele Identifier: CA645553269

Gene: GABRG2

Linked Data

• COSMIC: COSM6170314

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153237_162153238delinsTC , CM000667.2:g.162153237_162153238delinsTC	GRCh38
NC_000005.9:g.161580243_161580244delinsTC , CM000667.1:g.161580243_161580244delinsTC	GRCh37
NC_000005.8:g.161512821_161512822delinsTC	NCBI36
NG_009290.1:g.90596_90597delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1298_1299delinsTC
ENST00000361925.9:c.1393_1394delinsTC	ENSP00000354651.5:p.Arg465Ser
ENST00000523372.2:c.1356_1357delinsTC
ENST00000638253.1:n.551_552delinsTC
ENST00000638552.1:c.988_989delinsTC	ENSP00000491763.1:p.Arg330Ser
ENST00000638660.1:c.1012_1013delinsTC	ENSP00000492869.1:p.Arg338Ser
ENST00000638772.1:c.*3894_*3895delinsTC	ENSP00000491557.1:n.*3894_*3895delinsTC
ENST00000638877.1:c.1174_1175delinsTC
ENST00000639046.1:c.664_665delinsTC	ENSP00000492659.1:p.Arg222Ser
ENST00000639111.2:c.1273_1274delinsTC	ENSP00000492125.2:p.Arg425Ser
ENST00000639213.2:c.1297_1298delinsTC MANE Select	ENSP00000491909.2:p.Arg433Ser
ENST00000639278.1:c.1960_1961delinsTC	ENSP00000491958.1:n.1960_1961delinsTC
ENST00000639384.1:c.*1478_*1479delinsTC	ENSP00000491240.1:n.*1478_*1479delinsTC
ENST00000639424.1:c.*497_*498delinsTC	ENSP00000491245.1:n.*497_*498delinsTC
ENST00000639683.1:c.1231_1232delinsTC	ENSP00000492581.1:p.Arg411Ser
ENST00000639975.1:c.1207_1208delinsTC	ENSP00000492096.1:p.Arg403Ser
ENST00000640500.1:n.571_572delinsTC
ENST00000640739.1:n.6244_6245delinsTC
ENST00000640910.1:c.735_736delinsTC
ENST00000640985.1:c.1210_1211delinsTC	ENSP00000492293.1:p.Arg404Ser
ENST00000641017.1:c.1366_1367delinsTC	ENSP00000493461.1:p.Arg456Ser
ENST00000356592.7:c.1297_1298delinsTC	ENSP00000349000.3:p.Arg433Ser
ENST00000361925.8:c.1273_1274delinsTC	ENSP00000354651.4:p.Arg425Ser
ENST00000414552.6:c.1417_1418delinsTC	ENSP00000410732.2:p.Arg473Ser
ENST00000522990.5:c.*875_*876delinsTC	ENSP00000430732.1:n.*875_*876delinsTC
ENST00000523372.1:c.1394_1395delinsTC	ENSP00000430124.1:n.1394_1395delinsTC
NM_000816.3:c.1273_1274delinsTC	NP_000807.2:p.Arg425Ser
NM_198903.2:c.1417_1418delinsTC	NP_944493.2:p.Arg473Ser
NM_198904.2:c.1297_1298delinsTC	NP_944494.1:p.Arg433Ser
NM_001375339.1:c.1288_1289delinsTC	NP_001362268.1:p.Arg430Ser
NM_001375340.1:c.*131_*132delinsTC	NP_001362269.1:n.*131_*132delinsTC
NM_001375341.1:c.1294_1295delinsTC	NP_001362270.1:p.Arg432Ser
NM_001375342.1:c.1270_1271delinsTC	NP_001362271.1:p.Arg424Ser
NM_001375343.1:c.1393_1394delinsTC	NP_001362272.1:p.Arg465Ser
NM_001375344.1:c.1336_1337delinsTC	NP_001362273.1:p.Arg446Ser
NM_001375345.1:c.1207_1208delinsTC	NP_001362274.1:p.Arg403Ser
NM_001375346.1:c.1231_1232delinsTC	NP_001362275.1:p.Arg411Ser
NM_001375347.1:c.1210_1211delinsTC	NP_001362276.1:p.Arg404Ser
NM_001375348.1:c.853_854delinsTC	NP_001362277.1:p.Arg285Ser
NM_001375349.1:c.988_989delinsTC	NP_001362278.1:p.Arg330Ser
NM_001375350.1:c.877_878delinsTC	NP_001362279.1:p.Arg293Ser
NM_198904.3:c.1297_1298delinsTC	NP_944494.1:p.Arg433Ser
NM_198904.4:c.1297_1298delinsTC MANE Select	NP_944494.1:p.Arg433Ser