Canonical Allele Identifier: CA1596365207

Gene: GABRG2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162103918C= , CM000667.2:g.162103918C=	GRCh38
NC_000005.9:g.161530924C= , CM000667.1:g.161530924C=	GRCh37
NC_000005.8:g.161463502C=	NCBI36
NG_009290.1:g.41277C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.623C=
ENST00000361925.9:c.781C=	ENSP00000354651.5:p.Gln261=
ENST00000522053.2:n.552C=
ENST00000523372.2:c.744C=
ENST00000638552.1:c.376C=	ENSP00000491763.1:p.Gln126=
ENST00000638660.1:c.376C=	ENSP00000492869.1:p.Gln126=
ENST00000638772.1:c.661C=	ENSP00000491557.1:p.Gln221=
ENST00000638782.1:n.723C=
ENST00000638877.1:c.538C=
ENST00000639046.1:c.52C=	ENSP00000492659.1:p.Gln18=
ENST00000639111.2:c.661C=	ENSP00000492125.2:p.Gln221=
ENST00000639213.2:c.661C= MANE Select	ENSP00000491909.2:p.Gln221=
ENST00000639278.1:c.589C=	ENSP00000491958.1:p.Gln197=
ENST00000639384.1:c.661C=	ENSP00000491240.1:p.Gln221=
ENST00000639424.1:c.107+35812C=	ENSP00000491245.1:n.107+35812C=
ENST00000639683.1:c.595C=	ENSP00000492581.1:p.Gln199=
ENST00000639975.1:c.595C=	ENSP00000492096.1:p.Gln199=
ENST00000640574.1:c.376C=	ENSP00000491582.1:p.Gln126=
ENST00000640739.1:n.3192C=
ENST00000640910.1:c.99C=
ENST00000640985.1:c.574C=	ENSP00000492293.1:p.Gln192=
ENST00000641017.1:c.661C=	ENSP00000493461.1:p.Gln221=
ENST00000356592.7:c.661C=	ENSP00000349000.3:p.Gln221=
ENST00000361925.8:c.661C=	ENSP00000354651.4:p.Gln221=
ENST00000414552.6:c.781C=	ENSP00000410732.2:p.Gln261=
ENST00000522053.1:c.376C=	ENSP00000430182.1:p.Gln126=
ENST00000522990.5:c.*263C=	ENSP00000430732.1:n.*263C=
ENST00000523372.1:c.782C=	ENSP00000430124.1:n.782C=
NM_000816.3:c.661C=	NP_000807.2:p.Gln221=
NM_198903.2:c.781C=	NP_944493.2:p.Gln261=
NM_198904.2:c.661C=	NP_944494.1:p.Gln221=
NM_001375339.1:c.652C=	NP_001362268.1:p.Gln218=
NM_001375340.1:c.661C=	NP_001362269.1:p.Gln221=
NM_001375341.1:c.661C=	NP_001362270.1:p.Gln221=
NM_001375342.1:c.661C=	NP_001362271.1:p.Gln221=
NM_001375343.1:c.781C=	NP_001362272.1:p.Gln261=
NM_001375344.1:c.661C=	NP_001362273.1:p.Gln221=
NM_001375345.1:c.595C=	NP_001362274.1:p.Gln199=
NM_001375346.1:c.595C=	NP_001362275.1:p.Gln199=
NM_001375347.1:c.574C=	NP_001362276.1:p.Gln192=
NM_001375348.1:c.241C=	NP_001362277.1:p.Gln81=
NM_001375349.1:c.376C=	NP_001362278.1:p.Gln126=
NM_001375350.1:c.241C=	NP_001362279.1:p.Gln81=
NM_198904.3:c.661C=	NP_944494.1:p.Gln221=
NM_198904.4:c.661C= MANE Select	NP_944494.1:p.Gln221=