Canonical Allele Identifier: CA1596382104
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162153219T= , CM000667.2:g.162153219T= GRCh38
NC_000005.9:g.161580225T= , CM000667.1:g.161580225T= GRCh37
NC_000005.8:g.161512803T= NCBI36
NG_009290.1:g.90578T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.1280T=
ENST00000361925.9:c.1375T= ENSP00000354651.5:p.Cys459=
ENST00000523372.2:c.1338T=
ENST00000638253.1:n.533T=
ENST00000638552.1:c.970T= ENSP00000491763.1:p.Cys324=
ENST00000638660.1:c.994T= ENSP00000492869.1:p.Cys332=
ENST00000638772.1:c.*3876T= ENSP00000491557.1:n.*3876T=
ENST00000638877.1:c.1156T=
ENST00000639046.1:c.646T= ENSP00000492659.1:p.Cys216=
ENST00000639111.2:c.1255T= ENSP00000492125.2:p.Cys419=
ENST00000639213.2:c.1279T= MANE Select ENSP00000491909.2:p.Cys427=
ENST00000639278.1:c.1942T= ENSP00000491958.1:n.1942T=
ENST00000639384.1:c.*1460T= ENSP00000491240.1:n.*1460T=
ENST00000639424.1:c.*479T= ENSP00000491245.1:n.*479T=
ENST00000639683.1:c.1213T= ENSP00000492581.1:p.Cys405=
ENST00000639975.1:c.1189T= ENSP00000492096.1:p.Cys397=
ENST00000640500.1:n.553T=
ENST00000640739.1:n.6226T=
ENST00000640910.1:c.717T=
ENST00000640985.1:c.1192T= ENSP00000492293.1:p.Cys398=
ENST00000641017.1:c.1348T= ENSP00000493461.1:p.Cys450=
ENST00000356592.7:c.1279T= ENSP00000349000.3:p.Cys427=
ENST00000361925.8:c.1255T= ENSP00000354651.4:p.Cys419=
ENST00000414552.6:c.1399T= ENSP00000410732.2:p.Cys467=
ENST00000522990.5:c.*857T= ENSP00000430732.1:n.*857T=
ENST00000523372.1:c.1376T= ENSP00000430124.1:n.1376T=
NM_000816.3:c.1255T= NP_000807.2:p.Cys419=
NM_198903.2:c.1399T= NP_944493.2:p.Cys467=
NM_198904.2:c.1279T= NP_944494.1:p.Cys427=
NM_001375339.1:c.1270T= NP_001362268.1:p.Cys424=
NM_001375340.1:c.*113T= NP_001362269.1:n.*113T=
NM_001375341.1:c.1276T= NP_001362270.1:p.Cys426=
NM_001375342.1:c.1252T= NP_001362271.1:p.Cys418=
NM_001375343.1:c.1375T= NP_001362272.1:p.Cys459=
NM_001375344.1:c.1318T= NP_001362273.1:p.Cys440=
NM_001375345.1:c.1189T= NP_001362274.1:p.Cys397=
NM_001375346.1:c.1213T= NP_001362275.1:p.Cys405=
NM_001375347.1:c.1192T= NP_001362276.1:p.Cys398=
NM_001375348.1:c.835T= NP_001362277.1:p.Cys279=
NM_001375349.1:c.970T= NP_001362278.1:p.Cys324=
NM_001375350.1:c.859T= NP_001362279.1:p.Cys287=
NM_198904.3:c.1279T= NP_944494.1:p.Cys427=
NM_198904.4:c.1279T= MANE Select NP_944494.1:p.Cys427=