Canonical Allele Identifier: CA1596382083
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162153206T= , CM000667.2:g.162153206T= GRCh38
NC_000005.9:g.161580212T= , CM000667.1:g.161580212T= GRCh37
NC_000005.8:g.161512790T= NCBI36
NG_009290.1:g.90565T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.1267T=
ENST00000361925.9:c.1362T= ENSP00000354651.5:p.Cys454=
ENST00000523372.2:c.1325T=
ENST00000638253.1:n.520T=
ENST00000638552.1:c.957T= ENSP00000491763.1:p.Cys319=
ENST00000638660.1:c.981T= ENSP00000492869.1:p.Cys327=
ENST00000638772.1:c.*3863T= ENSP00000491557.1:n.*3863T=
ENST00000638877.1:c.1143T=
ENST00000639046.1:c.633T= ENSP00000492659.1:p.Cys211=
ENST00000639111.2:c.1242T= ENSP00000492125.2:p.Cys414=
ENST00000639213.2:c.1266T= MANE Select ENSP00000491909.2:p.Cys422=
ENST00000639278.1:c.1929T= ENSP00000491958.1:n.1929T=
ENST00000639384.1:c.*1447T= ENSP00000491240.1:n.*1447T=
ENST00000639424.1:c.*466T= ENSP00000491245.1:n.*466T=
ENST00000639683.1:c.1200T= ENSP00000492581.1:p.Cys400=
ENST00000639975.1:c.1176T= ENSP00000492096.1:p.Cys392=
ENST00000640500.1:n.540T=
ENST00000640739.1:n.6213T=
ENST00000640910.1:c.704T=
ENST00000640985.1:c.1179T= ENSP00000492293.1:p.Cys393=
ENST00000641017.1:c.1335T= ENSP00000493461.1:p.Cys445=
ENST00000356592.7:c.1266T= ENSP00000349000.3:p.Cys422=
ENST00000361925.8:c.1242T= ENSP00000354651.4:p.Cys414=
ENST00000414552.6:c.1386T= ENSP00000410732.2:p.Cys462=
ENST00000522990.5:c.*844T= ENSP00000430732.1:n.*844T=
ENST00000523372.1:c.1363T= ENSP00000430124.1:n.1363T=
NM_000816.3:c.1242T= NP_000807.2:p.Cys414=
NM_198903.2:c.1386T= NP_944493.2:p.Cys462=
NM_198904.2:c.1266T= NP_944494.1:p.Cys422=
NM_001375339.1:c.1257T= NP_001362268.1:p.Cys419=
NM_001375340.1:c.*100T= NP_001362269.1:n.*100T=
NM_001375341.1:c.1263T= NP_001362270.1:p.Cys421=
NM_001375342.1:c.1239T= NP_001362271.1:p.Cys413=
NM_001375343.1:c.1362T= NP_001362272.1:p.Cys454=
NM_001375344.1:c.1305T= NP_001362273.1:p.Cys435=
NM_001375345.1:c.1176T= NP_001362274.1:p.Cys392=
NM_001375346.1:c.1200T= NP_001362275.1:p.Cys400=
NM_001375347.1:c.1179T= NP_001362276.1:p.Cys393=
NM_001375348.1:c.822T= NP_001362277.1:p.Cys274=
NM_001375349.1:c.957T= NP_001362278.1:p.Cys319=
NM_001375350.1:c.846T= NP_001362279.1:p.Cys282=
NM_198904.3:c.1266T= NP_944494.1:p.Cys422=
NM_198904.4:c.1266T= MANE Select NP_944494.1:p.Cys422=