Canonical Allele Identifier: CA1596380237

Gene: GABRG2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162149143A= , CM000667.2:g.162149143A=	GRCh38
NC_000005.9:g.161576149A= , CM000667.1:g.161576149A=	GRCh37
NC_000005.8:g.161508727A=	NCBI36
NG_009290.1:g.86502A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.959A=
ENST00000361925.9:c.1078A=	ENSP00000354651.5:p.Thr360=
ENST00000522053.2:n.849A=
ENST00000523372.2:c.1041A=
ENST00000638253.1:n.212A=
ENST00000638552.1:c.673A=	ENSP00000491763.1:p.Thr225=
ENST00000638660.1:c.673A=	ENSP00000492869.1:p.Thr225=
ENST00000638772.1:c.958A=	ENSP00000491557.1:p.Thr320=
ENST00000638877.1:c.835A=
ENST00000639046.1:c.349A=	ENSP00000492659.1:p.Thr117=
ENST00000639111.2:c.958A=	ENSP00000492125.2:p.Thr320=
ENST00000639213.2:c.958A= MANE Select	ENSP00000491909.2:p.Thr320=
ENST00000639278.1:c.886A=	ENSP00000491958.1:p.Thr296=
ENST00000639384.1:c.958A=	ENSP00000491240.1:p.Thr320=
ENST00000639424.1:c.*158A=	ENSP00000491245.1:n.*158A=
ENST00000639683.1:c.892A=	ENSP00000492581.1:p.Thr298=
ENST00000639975.1:c.892A=	ENSP00000492096.1:p.Thr298=
ENST00000640500.1:n.256A=
ENST00000640574.1:c.673A=	ENSP00000491582.1:p.Thr225=
ENST00000640739.1:n.3489A=
ENST00000640910.1:c.396A=
ENST00000640985.1:c.871A=	ENSP00000492293.1:p.Thr291=
ENST00000641017.1:c.958A=	ENSP00000493461.1:p.Thr320=
ENST00000356592.7:c.958A=	ENSP00000349000.3:p.Thr320=
ENST00000361925.8:c.958A=	ENSP00000354651.4:p.Thr320=
ENST00000414552.6:c.1078A=	ENSP00000410732.2:p.Thr360=
ENST00000522990.5:c.*560A=	ENSP00000430732.1:n.*560A=
ENST00000523372.1:c.1079A=	ENSP00000430124.1:n.1079A=
NM_000816.3:c.958A=	NP_000807.2:p.Thr320=
NM_198903.2:c.1078A=	NP_944493.2:p.Thr360=
NM_198904.2:c.958A=	NP_944494.1:p.Thr320=
NM_001375339.1:c.949A=	NP_001362268.1:p.Thr317=
NM_001375340.1:c.923-2587A=	NP_001362269.1:n.923-2587A=
NM_001375341.1:c.955A=	NP_001362270.1:p.Thr319=
NM_001375342.1:c.955A=	NP_001362271.1:p.Thr319=
NM_001375343.1:c.1078A=	NP_001362272.1:p.Thr360=
NM_001375344.1:c.997A=	NP_001362273.1:p.Thr333=
NM_001375345.1:c.892A=	NP_001362274.1:p.Thr298=
NM_001375346.1:c.892A=	NP_001362275.1:p.Thr298=
NM_001375347.1:c.871A=	NP_001362276.1:p.Thr291=
NM_001375348.1:c.538A=	NP_001362277.1:p.Thr180=
NM_001375349.1:c.673A=	NP_001362278.1:p.Thr225=
NM_001375350.1:c.538A=	NP_001362279.1:p.Thr180=
NM_198904.3:c.958A=	NP_944494.1:p.Thr320=
NM_198904.4:c.958A= MANE Select	NP_944494.1:p.Thr320=