Canonical Allele Identifier: CA1596381972
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162153110C= , CM000667.2:g.162153110C= GRCh38
NC_000005.9:g.161580116C= , CM000667.1:g.161580116C= GRCh37
NC_000005.8:g.161512694C= NCBI36
NG_009290.1:g.90469C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.1171C=
ENST00000361925.9:c.1266C= ENSP00000354651.5:p.Ile422=
ENST00000523372.2:c.1229C=
ENST00000638253.1:n.424C=
ENST00000638552.1:c.861C= ENSP00000491763.1:p.Ile287=
ENST00000638660.1:c.885C= ENSP00000492869.1:p.Ile295=
ENST00000638772.1:c.*3767C= ENSP00000491557.1:n.*3767C=
ENST00000638877.1:c.1047C=
ENST00000639046.1:c.537C= ENSP00000492659.1:p.Ile179=
ENST00000639111.2:c.1146C= ENSP00000492125.2:p.Ile382=
ENST00000639213.2:c.1170C= MANE Select ENSP00000491909.2:p.Ile390=
ENST00000639278.1:c.1833C= ENSP00000491958.1:n.1833C=
ENST00000639384.1:c.*1351C= ENSP00000491240.1:n.*1351C=
ENST00000639424.1:c.*370C= ENSP00000491245.1:n.*370C=
ENST00000639683.1:c.1104C= ENSP00000492581.1:p.Ile368=
ENST00000639975.1:c.1080C= ENSP00000492096.1:p.Ile360=
ENST00000640500.1:n.444C=
ENST00000640739.1:n.6117C=
ENST00000640910.1:c.608C=
ENST00000640985.1:c.1083C= ENSP00000492293.1:p.Ile361=
ENST00000641017.1:c.1239C= ENSP00000493461.1:p.Ile413=
ENST00000356592.7:c.1170C= ENSP00000349000.3:p.Ile390=
ENST00000361925.8:c.1146C= ENSP00000354651.4:p.Ile382=
ENST00000414552.6:c.1290C= ENSP00000410732.2:p.Ile430=
ENST00000522990.5:c.*748C= ENSP00000430732.1:n.*748C=
ENST00000523372.1:c.1267C= ENSP00000430124.1:n.1267C=
NM_000816.3:c.1146C= NP_000807.2:p.Ile382=
NM_198903.2:c.1290C= NP_944493.2:p.Ile430=
NM_198904.2:c.1170C= NP_944494.1:p.Ile390=
NM_001375339.1:c.1161C= NP_001362268.1:p.Ile387=
NM_001375340.1:c.*4C= NP_001362269.1:n.*4C=
NM_001375341.1:c.1167C= NP_001362270.1:p.Ile389=
NM_001375342.1:c.1143C= NP_001362271.1:p.Ile381=
NM_001375343.1:c.1266C= NP_001362272.1:p.Ile422=
NM_001375344.1:c.1209C= NP_001362273.1:p.Ile403=
NM_001375345.1:c.1080C= NP_001362274.1:p.Ile360=
NM_001375346.1:c.1104C= NP_001362275.1:p.Ile368=
NM_001375347.1:c.1083C= NP_001362276.1:p.Ile361=
NM_001375348.1:c.726C= NP_001362277.1:p.Ile242=
NM_001375349.1:c.861C= NP_001362278.1:p.Ile287=
NM_001375350.1:c.750C= NP_001362279.1:p.Ile250=
NM_198904.3:c.1170C= NP_944494.1:p.Ile390=
NM_198904.4:c.1170C= MANE Select NP_944494.1:p.Ile390=