Canonical Allele Identifier: CA1596367438

Gene: GABRG2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162108758_162108759delinsAG , CM000667.2:g.162108758_162108759delinsAG	GRCh38
NC_000005.9:g.161535764_161535765delinsAG , CM000667.1:g.161535764_161535765delinsAG	GRCh37
NC_000005.8:g.161468342_161468343delinsAG	NCBI36
NG_009290.1:g.46117_46118delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.731+4732_731+4733delinsAG
ENST00000361925.9:c.889+4732_889+4733delinsAG	ENSP00000354651.5:n.889+4732_889+4733delinsAG
ENST00000522053.2:n.660+4732_660+4733delinsAG
ENST00000523372.2:c.852+4732_852+4733delinsAG
ENST00000638552.1:c.484+4732_484+4733delinsAG	ENSP00000491763.1:n.484+4732_484+4733delinsAG
ENST00000638660.1:c.484+4732_484+4733delinsAG	ENSP00000492869.1:n.484+4732_484+4733delinsAG
ENST00000638772.1:c.769+4732_769+4733delinsAG	ENSP00000491557.1:n.769+4732_769+4733delinsAG
ENST00000638782.1:n.831+4732_831+4733delinsAG
ENST00000638877.1:c.646+4732_646+4733delinsAG
ENST00000639046.1:c.160+4732_160+4733delinsAG	ENSP00000492659.1:n.160+4732_160+4733delinsAG
ENST00000639111.2:c.769+4732_769+4733delinsAG	ENSP00000492125.2:n.769+4732_769+4733delinsAG
ENST00000639213.2:c.769+4732_769+4733delinsAG MANE Select	ENSP00000491909.2:n.769+4732_769+4733delinsAG
ENST00000639278.1:c.697+4732_697+4733delinsAG	ENSP00000491958.1:n.697+4732_697+4733delinsAG
ENST00000639384.1:c.769+4732_769+4733delinsAG	ENSP00000491240.1:n.769+4732_769+4733delinsAG
ENST00000639424.1:c.108-33406_108-33405delinsAG	ENSP00000491245.1:n.108-33406_108-33405delinsAG
ENST00000639683.1:c.703+4732_703+4733delinsAG	ENSP00000492581.1:n.703+4732_703+4733delinsAG
ENST00000639975.1:c.703+4732_703+4733delinsAG	ENSP00000492096.1:n.703+4732_703+4733delinsAG
ENST00000640574.1:c.484+4732_484+4733delinsAG	ENSP00000491582.1:n.484+4732_484+4733delinsAG
ENST00000640739.1:n.3300+4732_3300+4733delinsAG
ENST00000640910.1:c.207+4732_207+4733delinsAG
ENST00000640985.1:c.682+4732_682+4733delinsAG	ENSP00000492293.1:n.682+4732_682+4733delinsAG
ENST00000641017.1:c.769+4732_769+4733delinsAG	ENSP00000493461.1:n.769+4732_769+4733delinsAG
ENST00000356592.7:c.769+4732_769+4733delinsAG	ENSP00000349000.3:n.769+4732_769+4733delinsAG
ENST00000361925.8:c.769+4732_769+4733delinsAG	ENSP00000354651.4:n.769+4732_769+4733delinsAG
ENST00000414552.6:c.889+4732_889+4733delinsAG	ENSP00000410732.2:n.889+4732_889+4733delinsAG
ENST00000522053.1:c.484+4732_484+4733delinsAG	ENSP00000430182.1:n.484+4732_484+4733delinsAG
ENST00000522990.5:c.*371+4732_*371+4733delinsAG	ENSP00000430732.1:n.*371+4732_*371+4733delinsAG
ENST00000523372.1:c.890+4732_890+4733delinsAG	ENSP00000430124.1:n.890+4732_890+4733delinsAG
NM_000816.3:c.769+4732_769+4733delinsAG	NP_000807.2:n.769+4732_769+4733delinsAG
NM_198903.2:c.889+4732_889+4733delinsAG	NP_944493.2:n.889+4732_889+4733delinsAG
NM_198904.2:c.769+4732_769+4733delinsAG	NP_944494.1:n.769+4732_769+4733delinsAG
NM_001375339.1:c.760+4732_760+4733delinsAG	NP_001362268.1:n.760+4732_760+4733delinsAG
NM_001375340.1:c.769+4732_769+4733delinsAG	NP_001362269.1:n.769+4732_769+4733delinsAG
NM_001375341.1:c.769+4732_769+4733delinsAG	NP_001362270.1:n.769+4732_769+4733delinsAG
NM_001375342.1:c.769+4732_769+4733delinsAG	NP_001362271.1:n.769+4732_769+4733delinsAG
NM_001375343.1:c.889+4732_889+4733delinsAG	NP_001362272.1:n.889+4732_889+4733delinsAG
NM_001375344.1:c.769+4732_769+4733delinsAG	NP_001362273.1:n.769+4732_769+4733delinsAG
NM_001375345.1:c.703+4732_703+4733delinsAG	NP_001362274.1:n.703+4732_703+4733delinsAG
NM_001375346.1:c.703+4732_703+4733delinsAG	NP_001362275.1:n.703+4732_703+4733delinsAG
NM_001375347.1:c.682+4732_682+4733delinsAG	NP_001362276.1:n.682+4732_682+4733delinsAG
NM_001375348.1:c.349+4732_349+4733delinsAG	NP_001362277.1:n.349+4732_349+4733delinsAG
NM_001375349.1:c.484+4732_484+4733delinsAG	NP_001362278.1:n.484+4732_484+4733delinsAG
NM_001375350.1:c.349+4732_349+4733delinsAG	NP_001362279.1:n.349+4732_349+4733delinsAG
NM_198904.3:c.769+4732_769+4733delinsAG	NP_944494.1:n.769+4732_769+4733delinsAG
NM_198904.4:c.769+4732_769+4733delinsAG MANE Select	NP_944494.1:n.769+4732_769+4733delinsAG