Canonical Allele Identifier: CA362182579

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161576247G>C (hg19) ; chr5:g.162149241G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162149241G>C , CM000667.2:g.162149241G>C	GRCh38
NC_000005.9:g.161576247G>C , CM000667.1:g.161576247G>C	GRCh37
NC_000005.8:g.161508825G>C	NCBI36
NG_009290.1:g.86600G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1057G>C
ENST00000361925.9:c.1176G>C	ENSP00000354651.5:p.Glu392Asp
ENST00000523372.2:c.1139G>C
ENST00000638253.1:n.310G>C
ENST00000638552.1:c.771G>C	ENSP00000491763.1:p.Glu257Asp
ENST00000638660.1:c.771G>C	ENSP00000492869.1:p.Glu257Asp
ENST00000638772.1:c.1056G>C	ENSP00000491557.1:p.Glu352Asp
ENST00000638877.1:c.933G>C
ENST00000639046.1:c.447G>C	ENSP00000492659.1:p.Glu149Asp
ENST00000639111.2:c.1056G>C	ENSP00000492125.2:p.Glu352Asp
ENST00000639213.2:c.1056G>C MANE Select	ENSP00000491909.2:p.Glu352Asp
ENST00000639278.1:c.984G>C	ENSP00000491958.1:p.Glu328Asp
ENST00000639384.1:c.1056G>C	ENSP00000491240.1:p.Glu352Asp
ENST00000639424.1:c.*256G>C	ENSP00000491245.1:n.*256G>C
ENST00000639683.1:c.990G>C	ENSP00000492581.1:p.Glu330Asp
ENST00000639975.1:c.990G>C	ENSP00000492096.1:p.Glu330Asp
ENST00000640500.1:n.354G>C
ENST00000640574.1:c.771G>C	ENSP00000491582.1:p.Glu257Asp
ENST00000640739.1:n.3587G>C
ENST00000640910.1:c.494G>C
ENST00000640985.1:c.969G>C	ENSP00000492293.1:p.Glu323Asp
ENST00000641017.1:c.1056G>C	ENSP00000493461.1:p.Glu352Asp
ENST00000356592.7:c.1056G>C	ENSP00000349000.3:p.Glu352Asp
ENST00000361925.8:c.1056G>C	ENSP00000354651.4:p.Glu352Asp
ENST00000414552.6:c.1176G>C	ENSP00000410732.2:p.Glu392Asp
ENST00000522990.5:c.*658G>C	ENSP00000430732.1:n.*658G>C
ENST00000523372.1:c.1177G>C	ENSP00000430124.1:n.1177G>C
NM_000816.3:c.1056G>C	NP_000807.2:p.Glu352Asp
NM_198903.2:c.1176G>C	NP_944493.2:p.Glu392Asp
NM_198904.2:c.1056G>C	NP_944494.1:p.Glu352Asp
NM_001375339.1:c.1047G>C	NP_001362268.1:p.Glu349Asp
NM_001375340.1:c.923-2489G>C	NP_001362269.1:n.923-2489G>C
NM_001375341.1:c.1053G>C	NP_001362270.1:p.Glu351Asp
NM_001375342.1:c.1053G>C	NP_001362271.1:p.Glu351Asp
NM_001375343.1:c.1176G>C	NP_001362272.1:p.Glu392Asp
NM_001375344.1:c.1095G>C	NP_001362273.1:p.Glu365Asp
NM_001375345.1:c.990G>C	NP_001362274.1:p.Glu330Asp
NM_001375346.1:c.990G>C	NP_001362275.1:p.Glu330Asp
NM_001375347.1:c.969G>C	NP_001362276.1:p.Glu323Asp
NM_001375348.1:c.636G>C	NP_001362277.1:p.Glu212Asp
NM_001375349.1:c.771G>C	NP_001362278.1:p.Glu257Asp
NM_001375350.1:c.636G>C	NP_001362279.1:p.Glu212Asp
NM_198904.3:c.1056G>C	NP_944494.1:p.Glu352Asp
NM_198904.4:c.1056G>C MANE Select	NP_944494.1:p.Glu352Asp