Canonical Allele Identifier: CA1596382089

Gene: GABRG2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153211_162153212delinsGT , CM000667.2:g.162153211_162153212delinsGT	GRCh38
NC_000005.9:g.161580217_161580218delinsGT , CM000667.1:g.161580217_161580218delinsGT	GRCh37
NC_000005.8:g.161512795_161512796delinsGT	NCBI36
NG_009290.1:g.90570_90571delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1272_1273delinsGT
ENST00000361925.9:c.1367_1368delinsGT	ENSP00000354651.5:p.Ser456=
ENST00000523372.2:c.1330_1331delinsGT
ENST00000638253.1:n.525_526delinsGT
ENST00000638552.1:c.962_963delinsGT	ENSP00000491763.1:p.Ser321=
ENST00000638660.1:c.986_987delinsGT	ENSP00000492869.1:p.Ser329=
ENST00000638772.1:c.*3868_*3869delinsGT	ENSP00000491557.1:n.*3868_*3869delinsGT
ENST00000638877.1:c.1148_1149delinsGT
ENST00000639046.1:c.638_639delinsGT	ENSP00000492659.1:p.Ser213=
ENST00000639111.2:c.1247_1248delinsGT	ENSP00000492125.2:p.Ser416=
ENST00000639213.2:c.1271_1272delinsGT MANE Select	ENSP00000491909.2:p.Ser424=
ENST00000639278.1:c.1934_1935delinsGT	ENSP00000491958.1:n.1934_1935delinsGT
ENST00000639384.1:c.*1452_*1453delinsGT	ENSP00000491240.1:n.*1452_*1453delinsGT
ENST00000639424.1:c.*471_*472delinsGT	ENSP00000491245.1:n.*471_*472delinsGT
ENST00000639683.1:c.1205_1206delinsGT	ENSP00000492581.1:p.Ser402=
ENST00000639975.1:c.1181_1182delinsGT	ENSP00000492096.1:p.Ser394=
ENST00000640500.1:n.545_546delinsGT
ENST00000640739.1:n.6218_6219delinsGT
ENST00000640910.1:c.709_710delinsGT
ENST00000640985.1:c.1184_1185delinsGT	ENSP00000492293.1:p.Ser395=
ENST00000641017.1:c.1340_1341delinsGT	ENSP00000493461.1:p.Ser447=
ENST00000356592.7:c.1271_1272delinsGT	ENSP00000349000.3:p.Ser424=
ENST00000361925.8:c.1247_1248delinsGT	ENSP00000354651.4:p.Ser416=
ENST00000414552.6:c.1391_1392delinsGT	ENSP00000410732.2:p.Ser464=
ENST00000522990.5:c.*849_*850delinsGT	ENSP00000430732.1:n.*849_*850delinsGT
ENST00000523372.1:c.1368_1369delinsGT	ENSP00000430124.1:n.1368_1369delinsGT
NM_000816.3:c.1247_1248delinsGT	NP_000807.2:p.Ser416=
NM_198903.2:c.1391_1392delinsGT	NP_944493.2:p.Ser464=
NM_198904.2:c.1271_1272delinsGT	NP_944494.1:p.Ser424=
NM_001375339.1:c.1262_1263delinsGT	NP_001362268.1:p.Ser421=
NM_001375340.1:c.*105_*106delinsGT	NP_001362269.1:n.*105_*106delinsGT
NM_001375341.1:c.1268_1269delinsGT	NP_001362270.1:p.Ser423=
NM_001375342.1:c.1244_1245delinsGT	NP_001362271.1:p.Ser415=
NM_001375343.1:c.1367_1368delinsGT	NP_001362272.1:p.Ser456=
NM_001375344.1:c.1310_1311delinsGT	NP_001362273.1:p.Ser437=
NM_001375345.1:c.1181_1182delinsGT	NP_001362274.1:p.Ser394=
NM_001375346.1:c.1205_1206delinsGT	NP_001362275.1:p.Ser402=
NM_001375347.1:c.1184_1185delinsGT	NP_001362276.1:p.Ser395=
NM_001375348.1:c.827_828delinsGT	NP_001362277.1:p.Ser276=
NM_001375349.1:c.962_963delinsGT	NP_001362278.1:p.Ser321=
NM_001375350.1:c.851_852delinsGT	NP_001362279.1:p.Ser284=
NM_198904.3:c.1271_1272delinsGT	NP_944494.1:p.Ser424=
NM_198904.4:c.1271_1272delinsGT MANE Select	NP_944494.1:p.Ser424=