Canonical Allele Identifier: CA1596382075

Gene: GABRG2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153197C= , CM000667.2:g.162153197C=	GRCh38
NC_000005.9:g.161580203C= , CM000667.1:g.161580203C=	GRCh37
NC_000005.8:g.161512781C=	NCBI36
NG_009290.1:g.90556C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1258C=
ENST00000361925.9:c.1353C=	ENSP00000354651.5:p.Gly451=
ENST00000523372.2:c.1316C=
ENST00000638253.1:n.511C=
ENST00000638552.1:c.948C=	ENSP00000491763.1:p.Gly316=
ENST00000638660.1:c.972C=	ENSP00000492869.1:p.Gly324=
ENST00000638772.1:c.*3854C=	ENSP00000491557.1:n.*3854C=
ENST00000638877.1:c.1134C=
ENST00000639046.1:c.624C=	ENSP00000492659.1:p.Gly208=
ENST00000639111.2:c.1233C=	ENSP00000492125.2:p.Gly411=
ENST00000639213.2:c.1257C= MANE Select	ENSP00000491909.2:p.Gly419=
ENST00000639278.1:c.1920C=	ENSP00000491958.1:n.1920C=
ENST00000639384.1:c.*1438C=	ENSP00000491240.1:n.*1438C=
ENST00000639424.1:c.*457C=	ENSP00000491245.1:n.*457C=
ENST00000639683.1:c.1191C=	ENSP00000492581.1:p.Gly397=
ENST00000639975.1:c.1167C=	ENSP00000492096.1:p.Gly389=
ENST00000640500.1:n.531C=
ENST00000640739.1:n.6204C=
ENST00000640910.1:c.695C=
ENST00000640985.1:c.1170C=	ENSP00000492293.1:p.Gly390=
ENST00000641017.1:c.1326C=	ENSP00000493461.1:p.Gly442=
ENST00000356592.7:c.1257C=	ENSP00000349000.3:p.Gly419=
ENST00000361925.8:c.1233C=	ENSP00000354651.4:p.Gly411=
ENST00000414552.6:c.1377C=	ENSP00000410732.2:p.Gly459=
ENST00000522990.5:c.*835C=	ENSP00000430732.1:n.*835C=
ENST00000523372.1:c.1354C=	ENSP00000430124.1:n.1354C=
NM_000816.3:c.1233C=	NP_000807.2:p.Gly411=
NM_198903.2:c.1377C=	NP_944493.2:p.Gly459=
NM_198904.2:c.1257C=	NP_944494.1:p.Gly419=
NM_001375339.1:c.1248C=	NP_001362268.1:p.Gly416=
NM_001375340.1:c.*91C=	NP_001362269.1:n.*91C=
NM_001375341.1:c.1254C=	NP_001362270.1:p.Gly418=
NM_001375342.1:c.1230C=	NP_001362271.1:p.Gly410=
NM_001375343.1:c.1353C=	NP_001362272.1:p.Gly451=
NM_001375344.1:c.1296C=	NP_001362273.1:p.Gly432=
NM_001375345.1:c.1167C=	NP_001362274.1:p.Gly389=
NM_001375346.1:c.1191C=	NP_001362275.1:p.Gly397=
NM_001375347.1:c.1170C=	NP_001362276.1:p.Gly390=
NM_001375348.1:c.813C=	NP_001362277.1:p.Gly271=
NM_001375349.1:c.948C=	NP_001362278.1:p.Gly316=
NM_001375350.1:c.837C=	NP_001362279.1:p.Gly279=
NM_198904.3:c.1257C=	NP_944494.1:p.Gly419=
NM_198904.4:c.1257C= MANE Select	NP_944494.1:p.Gly419=