Canonical Allele Identifier: CA1596365222

Gene: GABRG2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162103961G= , CM000667.2:g.162103961G=	GRCh38
NC_000005.9:g.161530967G= , CM000667.1:g.161530967G=	GRCh37
NC_000005.8:g.161463545G=	NCBI36
NG_009290.1:g.41320G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.666G=
ENST00000361925.9:c.824G=	ENSP00000354651.5:p.Trp275=
ENST00000522053.2:n.595G=
ENST00000523372.2:c.787G=
ENST00000638552.1:c.419G=	ENSP00000491763.1:p.Trp140=
ENST00000638660.1:c.419G=	ENSP00000492869.1:p.Trp140=
ENST00000638772.1:c.704G=	ENSP00000491557.1:p.Trp235=
ENST00000638782.1:n.766G=
ENST00000638877.1:c.581G=
ENST00000639046.1:c.95G=	ENSP00000492659.1:p.Trp32=
ENST00000639111.2:c.704G=	ENSP00000492125.2:p.Trp235=
ENST00000639213.2:c.704G= MANE Select	ENSP00000491909.2:p.Trp235=
ENST00000639278.1:c.632G=	ENSP00000491958.1:p.Trp211=
ENST00000639384.1:c.704G=	ENSP00000491240.1:p.Trp235=
ENST00000639424.1:c.107+35855G=	ENSP00000491245.1:n.107+35855G=
ENST00000639683.1:c.638G=	ENSP00000492581.1:p.Trp213=
ENST00000639975.1:c.638G=	ENSP00000492096.1:p.Trp213=
ENST00000640574.1:c.419G=	ENSP00000491582.1:p.Trp140=
ENST00000640739.1:n.3235G=
ENST00000640910.1:c.142G=
ENST00000640985.1:c.617G=	ENSP00000492293.1:p.Trp206=
ENST00000641017.1:c.704G=	ENSP00000493461.1:p.Trp235=
ENST00000356592.7:c.704G=	ENSP00000349000.3:p.Trp235=
ENST00000361925.8:c.704G=	ENSP00000354651.4:p.Trp235=
ENST00000414552.6:c.824G=	ENSP00000410732.2:p.Trp275=
ENST00000522053.1:c.419G=	ENSP00000430182.1:p.Trp140=
ENST00000522990.5:c.*306G=	ENSP00000430732.1:n.*306G=
ENST00000523372.1:c.825G=	ENSP00000430124.1:n.825G=
NM_000816.3:c.704G=	NP_000807.2:p.Trp235=
NM_198903.2:c.824G=	NP_944493.2:p.Trp275=
NM_198904.2:c.704G=	NP_944494.1:p.Trp235=
NM_001375339.1:c.695G=	NP_001362268.1:p.Trp232=
NM_001375340.1:c.704G=	NP_001362269.1:p.Trp235=
NM_001375341.1:c.704G=	NP_001362270.1:p.Trp235=
NM_001375342.1:c.704G=	NP_001362271.1:p.Trp235=
NM_001375343.1:c.824G=	NP_001362272.1:p.Trp275=
NM_001375344.1:c.704G=	NP_001362273.1:p.Trp235=
NM_001375345.1:c.638G=	NP_001362274.1:p.Trp213=
NM_001375346.1:c.638G=	NP_001362275.1:p.Trp213=
NM_001375347.1:c.617G=	NP_001362276.1:p.Trp206=
NM_001375348.1:c.284G=	NP_001362277.1:p.Trp95=
NM_001375349.1:c.419G=	NP_001362278.1:p.Trp140=
NM_001375350.1:c.284G=	NP_001362279.1:p.Trp95=
NM_198904.3:c.704G=	NP_944494.1:p.Trp235=
NM_198904.4:c.704G= MANE Select	NP_944494.1:p.Trp235=