Canonical Allele Identifier: CA1596382376

Gene: GABRG2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153409T= , CM000667.2:g.162153409T=	GRCh38
NC_000005.9:g.161580415T= , CM000667.1:g.161580415T=	GRCh37
NC_000005.8:g.161512993T=	NCBI36
NG_009290.1:g.90768T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1470T=
ENST00000361925.9:c.*41T=	ENSP00000354651.5:n.*41T=
ENST00000523372.2:c.1528T=
ENST00000638253.1:n.723T=
ENST00000638552.1:c.*41T=	ENSP00000491763.1:n.*41T=
ENST00000638660.1:c.*41T=	ENSP00000492869.1:n.*41T=
ENST00000638772.1:c.*4066T=	ENSP00000491557.1:n.*4066T=
ENST00000638877.1:c.1346T=
ENST00000639046.1:c.*41T=	ENSP00000492659.1:n.*41T=
ENST00000639111.2:c.*41T=	ENSP00000492125.2:n.*41T=
ENST00000639213.2:c.*41T= MANE Select	ENSP00000491909.2:n.*41T=
ENST00000639278.1:c.2132T=	ENSP00000491958.1:n.2132T=
ENST00000639384.1:c.*1650T=	ENSP00000491240.1:n.*1650T=
ENST00000639424.1:c.*669T=	ENSP00000491245.1:n.*669T=
ENST00000639683.1:c.*41T=	ENSP00000492581.1:n.*41T=
ENST00000639975.1:c.*41T=	ENSP00000492096.1:n.*41T=
ENST00000640500.1:n.743T=
ENST00000640739.1:n.6416T=
ENST00000640910.1:c.907T=
ENST00000640985.1:c.*41T=	ENSP00000492293.1:n.*41T=
ENST00000641017.1:c.1538T=	ENSP00000493461.1:n.1538T=
ENST00000356592.7:c.*41T=	ENSP00000349000.3:n.*41T=
ENST00000361925.8:c.*41T=	ENSP00000354651.4:n.*41T=
ENST00000414552.6:c.*41T=	ENSP00000410732.2:n.*41T=
ENST00000522990.5:c.*1047T=	ENSP00000430732.1:n.*1047T=
ENST00000523372.1:c.1566T=	ENSP00000430124.1:n.1566T=
NM_000816.3:c.*41T=	NP_000807.2:n.*41T=
NM_198903.2:c.*41T=	NP_944493.2:n.*41T=
NM_198904.2:c.*41T=	NP_944494.1:n.*41T=
NM_001375339.1:c.*41T=	NP_001362268.1:n.*41T=
NM_001375340.1:c.*303T=	NP_001362269.1:n.*303T=
NM_001375341.1:c.*41T=	NP_001362270.1:n.*41T=
NM_001375342.1:c.*41T=	NP_001362271.1:n.*41T=
NM_001375343.1:c.*41T=	NP_001362272.1:n.*41T=
NM_001375344.1:c.*41T=	NP_001362273.1:n.*41T=
NM_001375345.1:c.*41T=	NP_001362274.1:n.*41T=
NM_001375346.1:c.*41T=	NP_001362275.1:n.*41T=
NM_001375347.1:c.*41T=	NP_001362276.1:n.*41T=
NM_001375348.1:c.*41T=	NP_001362277.1:n.*41T=
NM_001375349.1:c.*41T=	NP_001362278.1:n.*41T=
NM_001375350.1:c.*41T=	NP_001362279.1:n.*41T=
NM_198904.3:c.*41T=	NP_944494.1:n.*41T=
NM_198904.4:c.*41T= MANE Select	NP_944494.1:n.*41T=