Canonical Allele Identifier: CA1596382164
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162153271T= , CM000667.2:g.162153271T= GRCh38
NC_000005.9:g.161580277T= , CM000667.1:g.161580277T= GRCh37
NC_000005.8:g.161512855T= NCBI36
NG_009290.1:g.90630T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.1332T=
ENST00000361925.9:c.1427T= ENSP00000354651.5:p.Ile476=
ENST00000523372.2:c.1390T=
ENST00000638253.1:n.585T=
ENST00000638552.1:c.1022T= ENSP00000491763.1:p.Ile341=
ENST00000638660.1:c.1046T= ENSP00000492869.1:p.Ile349=
ENST00000638772.1:c.*3928T= ENSP00000491557.1:n.*3928T=
ENST00000638877.1:c.1208T=
ENST00000639046.1:c.698T= ENSP00000492659.1:p.Ile233=
ENST00000639111.2:c.1307T= ENSP00000492125.2:p.Ile436=
ENST00000639213.2:c.1331T= MANE Select ENSP00000491909.2:p.Ile444=
ENST00000639278.1:c.1994T= ENSP00000491958.1:n.1994T=
ENST00000639384.1:c.*1512T= ENSP00000491240.1:n.*1512T=
ENST00000639424.1:c.*531T= ENSP00000491245.1:n.*531T=
ENST00000639683.1:c.1265T= ENSP00000492581.1:p.Ile422=
ENST00000639975.1:c.1241T= ENSP00000492096.1:p.Ile414=
ENST00000640500.1:n.605T=
ENST00000640739.1:n.6278T=
ENST00000640910.1:c.769T=
ENST00000640985.1:c.1244T= ENSP00000492293.1:p.Ile415=
ENST00000641017.1:c.1400T= ENSP00000493461.1:p.Ile467=
ENST00000356592.7:c.1331T= ENSP00000349000.3:p.Ile444=
ENST00000361925.8:c.1307T= ENSP00000354651.4:p.Ile436=
ENST00000414552.6:c.1451T= ENSP00000410732.2:p.Ile484=
ENST00000522990.5:c.*909T= ENSP00000430732.1:n.*909T=
ENST00000523372.1:c.1428T= ENSP00000430124.1:n.1428T=
NM_000816.3:c.1307T= NP_000807.2:p.Ile436=
NM_198903.2:c.1451T= NP_944493.2:p.Ile484=
NM_198904.2:c.1331T= NP_944494.1:p.Ile444=
NM_001375339.1:c.1322T= NP_001362268.1:p.Ile441=
NM_001375340.1:c.*165T= NP_001362269.1:n.*165T=
NM_001375341.1:c.1328T= NP_001362270.1:p.Ile443=
NM_001375342.1:c.1304T= NP_001362271.1:p.Ile435=
NM_001375343.1:c.1427T= NP_001362272.1:p.Ile476=
NM_001375344.1:c.1370T= NP_001362273.1:p.Ile457=
NM_001375345.1:c.1241T= NP_001362274.1:p.Ile414=
NM_001375346.1:c.1265T= NP_001362275.1:p.Ile422=
NM_001375347.1:c.1244T= NP_001362276.1:p.Ile415=
NM_001375348.1:c.887T= NP_001362277.1:p.Ile296=
NM_001375349.1:c.1022T= NP_001362278.1:p.Ile341=
NM_001375350.1:c.911T= NP_001362279.1:p.Ile304=
NM_198904.3:c.1331T= NP_944494.1:p.Ile444=
NM_198904.4:c.1331T= MANE Select NP_944494.1:p.Ile444=