Canonical Allele Identifier: CA1596380258

Gene: GABRG2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162149187G= , CM000667.2:g.162149187G=	GRCh38
NC_000005.9:g.161576193G= , CM000667.1:g.161576193G=	GRCh37
NC_000005.8:g.161508771G=	NCBI36
NG_009290.1:g.86546G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1003G=
ENST00000361925.9:c.1122G=	ENSP00000354651.5:p.Ala374=
ENST00000523372.2:c.1085G=
ENST00000638253.1:n.256G=
ENST00000638552.1:c.717G=	ENSP00000491763.1:p.Ala239=
ENST00000638660.1:c.717G=	ENSP00000492869.1:p.Ala239=
ENST00000638772.1:c.1002G=	ENSP00000491557.1:p.Ala334=
ENST00000638877.1:c.879G=
ENST00000639046.1:c.393G=	ENSP00000492659.1:p.Ala131=
ENST00000639111.2:c.1002G=	ENSP00000492125.2:p.Ala334=
ENST00000639213.2:c.1002G= MANE Select	ENSP00000491909.2:p.Ala334=
ENST00000639278.1:c.930G=	ENSP00000491958.1:p.Ala310=
ENST00000639384.1:c.1002G=	ENSP00000491240.1:p.Ala334=
ENST00000639424.1:c.*202G=	ENSP00000491245.1:n.*202G=
ENST00000639683.1:c.936G=	ENSP00000492581.1:p.Ala312=
ENST00000639975.1:c.936G=	ENSP00000492096.1:p.Ala312=
ENST00000640500.1:n.300G=
ENST00000640574.1:c.717G=	ENSP00000491582.1:p.Ala239=
ENST00000640739.1:n.3533G=
ENST00000640910.1:c.440G=
ENST00000640985.1:c.915G=	ENSP00000492293.1:p.Ala305=
ENST00000641017.1:c.1002G=	ENSP00000493461.1:p.Ala334=
ENST00000356592.7:c.1002G=	ENSP00000349000.3:p.Ala334=
ENST00000361925.8:c.1002G=	ENSP00000354651.4:p.Ala334=
ENST00000414552.6:c.1122G=	ENSP00000410732.2:p.Ala374=
ENST00000522990.5:c.*604G=	ENSP00000430732.1:n.*604G=
ENST00000523372.1:c.1123G=	ENSP00000430124.1:n.1123G=
NM_000816.3:c.1002G=	NP_000807.2:p.Ala334=
NM_198903.2:c.1122G=	NP_944493.2:p.Ala374=
NM_198904.2:c.1002G=	NP_944494.1:p.Ala334=
NM_001375339.1:c.993G=	NP_001362268.1:p.Ala331=
NM_001375340.1:c.923-2543G=	NP_001362269.1:n.923-2543G=
NM_001375341.1:c.999G=	NP_001362270.1:p.Ala333=
NM_001375342.1:c.999G=	NP_001362271.1:p.Ala333=
NM_001375343.1:c.1122G=	NP_001362272.1:p.Ala374=
NM_001375344.1:c.1041G=	NP_001362273.1:p.Ala347=
NM_001375345.1:c.936G=	NP_001362274.1:p.Ala312=
NM_001375346.1:c.936G=	NP_001362275.1:p.Ala312=
NM_001375347.1:c.915G=	NP_001362276.1:p.Ala305=
NM_001375348.1:c.582G=	NP_001362277.1:p.Ala194=
NM_001375349.1:c.717G=	NP_001362278.1:p.Ala239=
NM_001375350.1:c.582G=	NP_001362279.1:p.Ala194=
NM_198904.3:c.1002G=	NP_944494.1:p.Ala334=
NM_198904.4:c.1002G= MANE Select	NP_944494.1:p.Ala334=