Canonical Allele Identifier: CA650531524

Gene: GABRG2

Linked Data

• COSMIC: COSN19710551

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153369_162153370insT , CM000667.2:g.162153369_162153370insT	GRCh38
NC_000005.9:g.161580375_161580376insT , CM000667.1:g.161580375_161580376insT	GRCh37
NC_000005.8:g.161512953_161512954insT	NCBI36
NG_009290.1:g.90728_90729insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1430_1431insT
ENST00000361925.9:c.*1_*2insT	ENSP00000354651.5:n.*1_*2insT
ENST00000523372.2:c.1488_1489insT
ENST00000638253.1:n.683_684insT
ENST00000638552.1:c.*1_*2insT	ENSP00000491763.1:n.*1_*2insT
ENST00000638660.1:c.*1_*2insT	ENSP00000492869.1:n.*1_*2insT
ENST00000638772.1:c.*4026_*4027insT	ENSP00000491557.1:n.*4026_*4027insT
ENST00000638877.1:c.1306_1307insT
ENST00000639046.1:c.*1_*2insT	ENSP00000492659.1:n.*1_*2insT
ENST00000639111.2:c.*1_*2insT	ENSP00000492125.2:n.*1_*2insT
ENST00000639213.2:c.*1_*2insT MANE Select	ENSP00000491909.2:n.*1_*2insT
ENST00000639278.1:c.2092_2093insT	ENSP00000491958.1:n.2092_2093insT
ENST00000639384.1:c.*1610_*1611insT	ENSP00000491240.1:n.*1610_*1611insT
ENST00000639424.1:c.*629_*630insT	ENSP00000491245.1:n.*629_*630insT
ENST00000639683.1:c.*1_*2insT	ENSP00000492581.1:n.*1_*2insT
ENST00000639975.1:c.*1_*2insT	ENSP00000492096.1:n.*1_*2insT
ENST00000640500.1:n.703_704insT
ENST00000640739.1:n.6376_6377insT
ENST00000640910.1:c.867_868insT
ENST00000640985.1:c.*1_*2insT	ENSP00000492293.1:n.*1_*2insT
ENST00000641017.1:c.1498_1499insT	ENSP00000493461.1:n.1498_1499insT
ENST00000356592.7:c.*1_*2insT	ENSP00000349000.3:n.*1_*2insT
ENST00000361925.8:c.*1_*2insT	ENSP00000354651.4:n.*1_*2insT
ENST00000414552.6:c.*1_*2insT	ENSP00000410732.2:n.*1_*2insT
ENST00000522990.5:c.*1007_*1008insT	ENSP00000430732.1:n.*1007_*1008insT
ENST00000523372.1:c.1526_1527insT	ENSP00000430124.1:n.1526_1527insT
NM_000816.3:c.*1_*2insT	NP_000807.2:n.*1_*2insT
NM_198903.2:c.*1_*2insT	NP_944493.2:n.*1_*2insT
NM_198904.2:c.*1_*2insT	NP_944494.1:n.*1_*2insT
NM_001375339.1:c.*1_*2insT	NP_001362268.1:n.*1_*2insT
NM_001375340.1:c.*263_*264insT	NP_001362269.1:n.*263_*264insT
NM_001375341.1:c.*1_*2insT	NP_001362270.1:n.*1_*2insT
NM_001375342.1:c.*1_*2insT	NP_001362271.1:n.*1_*2insT
NM_001375343.1:c.*1_*2insT	NP_001362272.1:n.*1_*2insT
NM_001375344.1:c.*1_*2insT	NP_001362273.1:n.*1_*2insT
NM_001375345.1:c.*1_*2insT	NP_001362274.1:n.*1_*2insT
NM_001375346.1:c.*1_*2insT	NP_001362275.1:n.*1_*2insT
NM_001375347.1:c.*1_*2insT	NP_001362276.1:n.*1_*2insT
NM_001375348.1:c.*1_*2insT	NP_001362277.1:n.*1_*2insT
NM_001375349.1:c.*1_*2insT	NP_001362278.1:n.*1_*2insT
NM_001375350.1:c.*1_*2insT	NP_001362279.1:n.*1_*2insT
NM_198904.3:c.*1_*2insT	NP_944494.1:n.*1_*2insT
NM_198904.4:c.*1_*2insT MANE Select	NP_944494.1:n.*1_*2insT