Canonical Allele Identifier: CA362183772

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161580258A>G (hg19) ; chr5:g.162153252A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153252A>G , CM000667.2:g.162153252A>G	GRCh38
NC_000005.9:g.161580258A>G , CM000667.1:g.161580258A>G	GRCh37
NC_000005.8:g.161512836A>G	NCBI36
NG_009290.1:g.90611A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1313A>G
ENST00000361925.9:c.1408A>G	ENSP00000354651.5:p.Arg470Gly
ENST00000523372.2:c.1371A>G
ENST00000638253.1:n.566A>G
ENST00000638552.1:c.1003A>G	ENSP00000491763.1:p.Arg335Gly
ENST00000638660.1:c.1027A>G	ENSP00000492869.1:p.Arg343Gly
ENST00000638772.1:c.*3909A>G	ENSP00000491557.1:n.*3909A>G
ENST00000638877.1:c.1189A>G
ENST00000639046.1:c.679A>G	ENSP00000492659.1:p.Arg227Gly
ENST00000639111.2:c.1288A>G	ENSP00000492125.2:p.Arg430Gly
ENST00000639213.2:c.1312A>G MANE Select	ENSP00000491909.2:p.Arg438Gly
ENST00000639278.1:c.1975A>G	ENSP00000491958.1:n.1975A>G
ENST00000639384.1:c.*1493A>G	ENSP00000491240.1:n.*1493A>G
ENST00000639424.1:c.*512A>G	ENSP00000491245.1:n.*512A>G
ENST00000639683.1:c.1246A>G	ENSP00000492581.1:p.Arg416Gly
ENST00000639975.1:c.1222A>G	ENSP00000492096.1:p.Arg408Gly
ENST00000640500.1:n.586A>G
ENST00000640739.1:n.6259A>G
ENST00000640910.1:c.750A>G
ENST00000640985.1:c.1225A>G	ENSP00000492293.1:p.Arg409Gly
ENST00000641017.1:c.1381A>G	ENSP00000493461.1:p.Arg461Gly
ENST00000356592.7:c.1312A>G	ENSP00000349000.3:p.Arg438Gly
ENST00000361925.8:c.1288A>G	ENSP00000354651.4:p.Arg430Gly
ENST00000414552.6:c.1432A>G	ENSP00000410732.2:p.Arg478Gly
ENST00000522990.5:c.*890A>G	ENSP00000430732.1:n.*890A>G
ENST00000523372.1:c.1409A>G	ENSP00000430124.1:n.1409A>G
NM_000816.3:c.1288A>G	NP_000807.2:p.Arg430Gly
NM_198903.2:c.1432A>G	NP_944493.2:p.Arg478Gly
NM_198904.2:c.1312A>G	NP_944494.1:p.Arg438Gly
NM_001375339.1:c.1303A>G	NP_001362268.1:p.Arg435Gly
NM_001375340.1:c.*146A>G	NP_001362269.1:n.*146A>G
NM_001375341.1:c.1309A>G	NP_001362270.1:p.Arg437Gly
NM_001375342.1:c.1285A>G	NP_001362271.1:p.Arg429Gly
NM_001375343.1:c.1408A>G	NP_001362272.1:p.Arg470Gly
NM_001375344.1:c.1351A>G	NP_001362273.1:p.Arg451Gly
NM_001375345.1:c.1222A>G	NP_001362274.1:p.Arg408Gly
NM_001375346.1:c.1246A>G	NP_001362275.1:p.Arg416Gly
NM_001375347.1:c.1225A>G	NP_001362276.1:p.Arg409Gly
NM_001375348.1:c.868A>G	NP_001362277.1:p.Arg290Gly
NM_001375349.1:c.1003A>G	NP_001362278.1:p.Arg335Gly
NM_001375350.1:c.892A>G	NP_001362279.1:p.Arg298Gly
NM_198904.3:c.1312A>G	NP_944494.1:p.Arg438Gly
NM_198904.4:c.1312A>G MANE Select	NP_944494.1:p.Arg438Gly