Canonical Allele Identifier: CA1596380285

Gene: GABRG2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162149281A= , CM000667.2:g.162149281A=	GRCh38
NC_000005.9:g.161576287A= , CM000667.1:g.161576287A=	GRCh37
NC_000005.8:g.161508865A=	NCBI36
NG_009290.1:g.86640A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1097A=
ENST00000361925.9:c.1216A=	ENSP00000354651.5:p.Ser406=
ENST00000523372.2:c.1179A=
ENST00000638253.1:n.350A=
ENST00000638552.1:c.811A=	ENSP00000491763.1:p.Ser271=
ENST00000638660.1:c.811A=	ENSP00000492869.1:p.Ser271=
ENST00000638772.1:c.1096A=	ENSP00000491557.1:p.Ser366=
ENST00000638877.1:c.973A=
ENST00000639046.1:c.487A=	ENSP00000492659.1:p.Ser163=
ENST00000639111.2:c.1096A=	ENSP00000492125.2:p.Ser366=
ENST00000639213.2:c.1096A= MANE Select	ENSP00000491909.2:p.Ser366=
ENST00000639278.1:c.1024A=	ENSP00000491958.1:p.Ser342=
ENST00000639384.1:c.1096A=	ENSP00000491240.1:p.Ser366=
ENST00000639424.1:c.*296A=	ENSP00000491245.1:n.*296A=
ENST00000639683.1:c.1030A=	ENSP00000492581.1:p.Ser344=
ENST00000639975.1:c.1030A=	ENSP00000492096.1:p.Ser344=
ENST00000640500.1:n.394A=
ENST00000640574.1:c.811A=	ENSP00000491582.1:p.Ser271=
ENST00000640739.1:n.3627A=
ENST00000640910.1:c.534A=
ENST00000640985.1:c.1009A=	ENSP00000492293.1:p.Ser337=
ENST00000641017.1:c.1096A=	ENSP00000493461.1:p.Ser366=
ENST00000356592.7:c.1096A=	ENSP00000349000.3:p.Ser366=
ENST00000361925.8:c.1096A=	ENSP00000354651.4:p.Ser366=
ENST00000414552.6:c.1216A=	ENSP00000410732.2:p.Ser406=
ENST00000522990.5:c.*698A=	ENSP00000430732.1:n.*698A=
ENST00000523372.1:c.1217A=	ENSP00000430124.1:n.1217A=
NM_000816.3:c.1096A=	NP_000807.2:p.Ser366=
NM_198903.2:c.1216A=	NP_944493.2:p.Ser406=
NM_198904.2:c.1096A=	NP_944494.1:p.Ser366=
NM_001375339.1:c.1087A=	NP_001362268.1:p.Ser363=
NM_001375340.1:c.923-2449A=	NP_001362269.1:n.923-2449A=
NM_001375341.1:c.1093A=	NP_001362270.1:p.Ser365=
NM_001375342.1:c.1093A=	NP_001362271.1:p.Ser365=
NM_001375343.1:c.1216A=	NP_001362272.1:p.Ser406=
NM_001375344.1:c.1135A=	NP_001362273.1:p.Ser379=
NM_001375345.1:c.1030A=	NP_001362274.1:p.Ser344=
NM_001375346.1:c.1030A=	NP_001362275.1:p.Ser344=
NM_001375347.1:c.1009A=	NP_001362276.1:p.Ser337=
NM_001375348.1:c.676A=	NP_001362277.1:p.Ser226=
NM_001375349.1:c.811A=	NP_001362278.1:p.Ser271=
NM_001375350.1:c.676A=	NP_001362279.1:p.Ser226=
NM_198904.3:c.1096A=	NP_944494.1:p.Ser366=
NM_198904.4:c.1096A= MANE Select	NP_944494.1:p.Ser366=