Canonical Allele Identifier: CA2580614790
Gene: GABRG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1928713
ClinVar RCV Id: RCV002635114

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162149304_162149306del , CM000667.2:g.162149304_162149306del GRCh38
NC_000005.9:g.161576310_161576312del , CM000667.1:g.161576310_161576312del GRCh37
NC_000005.8:g.161508888_161508890del NCBI36
NG_009290.1:g.86663_86665del

Transcript Alleles

HGVS Amino-acid change
ENST00000356592.8:c.1120_1122del
ENST00000361925.9:c.1239_1241del ENSP00000354651.5:p.Lys414del
ENST00000523372.2:c.1202_1204del
ENST00000638253.1:n.373_375del
ENST00000638552.1:c.834_836del ENSP00000491763.1:p.Lys279del
ENST00000638660.1:c.834_836del ENSP00000492869.1:p.Lys279del
ENST00000638772.1:c.1119_1121del ENSP00000491557.1:p.Lys374del
ENST00000638877.1:c.996_998del
ENST00000639046.1:c.510_512del ENSP00000492659.1:p.Lys171del
ENST00000639111.2:c.1119_1121del ENSP00000492125.2:p.Lys374del
ENST00000639213.2:c.1119_1121del MANE Select ENSP00000491909.2:p.Lys374del
ENST00000639278.1:c.1047_1049del ENSP00000491958.1:p.Lys350del
ENST00000639384.1:c.1119_1121del ENSP00000491240.1:p.Lys374del
ENST00000639424.1:c.*319_*321del ENSP00000491245.1:n.*319_*321del
ENST00000639683.1:c.1053_1055del ENSP00000492581.1:p.Lys352del
ENST00000639975.1:c.1053_1055del ENSP00000492096.1:p.Lys352del
ENST00000640500.1:n.417_419del
ENST00000640574.1:c.834_836del ENSP00000491582.1:p.Lys279del
ENST00000640739.1:n.3650_3652del
ENST00000640910.1:c.557_559del
ENST00000640985.1:c.1032_1034del ENSP00000492293.1:p.Lys345del
ENST00000641017.1:c.1119_1121del ENSP00000493461.1:p.Lys374del
ENST00000356592.7:c.1119_1121del ENSP00000349000.3:p.Lys374del
ENST00000361925.8:c.1119_1121del ENSP00000354651.4:p.Lys374del
ENST00000414552.6:c.1239_1241del ENSP00000410732.2:p.Lys414del
ENST00000522990.5:c.*721_*723del ENSP00000430732.1:n.*721_*723del
ENST00000523372.1:c.1240_1242del ENSP00000430124.1:n.1240_1242del
NM_000816.3:c.1119_1121del NP_000807.2:p.Lys374del
NM_198903.2:c.1239_1241del NP_944493.2:p.Lys414del
NM_198904.2:c.1119_1121del NP_944494.1:p.Lys374del
NM_001375339.1:c.1110_1112del NP_001362268.1:p.Lys371del
NM_001375340.1:c.923-2426_923-2424del NP_001362269.1:n.923-2426_923-2424del
NM_001375341.1:c.1116_1118del NP_001362270.1:p.Lys373del
NM_001375342.1:c.1116_1118del NP_001362271.1:p.Lys373del
NM_001375343.1:c.1239_1241del NP_001362272.1:p.Lys414del
NM_001375344.1:c.1158_1160del NP_001362273.1:p.Lys387del
NM_001375345.1:c.1053_1055del NP_001362274.1:p.Lys352del
NM_001375346.1:c.1053_1055del NP_001362275.1:p.Lys352del
NM_001375347.1:c.1032_1034del NP_001362276.1:p.Lys345del
NM_001375348.1:c.699_701del NP_001362277.1:p.Lys234del
NM_001375349.1:c.834_836del NP_001362278.1:p.Lys279del
NM_001375350.1:c.699_701del NP_001362279.1:p.Lys234del
NM_198904.3:c.1119_1121del NP_944494.1:p.Lys374del
NM_198904.4:c.1119_1121del MANE Select NP_944494.1:p.Lys374del