Canonical Allele Identifier: CA362184137
Gene: GABRG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162153337T>C , CM000667.2:g.162153337T>C GRCh38
NC_000005.9:g.161580343T>C , CM000667.1:g.161580343T>C GRCh37
NC_000005.8:g.161512921T>C NCBI36
NG_009290.1:g.90696T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.1398T>C
ENST00000361925.9:c.1493T>C ENSP00000354651.5:p.Leu498Pro
ENST00000523372.2:c.1456T>C
ENST00000638253.1:n.651T>C
ENST00000638552.1:c.1088T>C ENSP00000491763.1:p.Leu363Pro
ENST00000638660.1:c.1112T>C ENSP00000492869.1:p.Leu371Pro
ENST00000638772.1:c.*3994T>C ENSP00000491557.1:n.*3994T>C
ENST00000638877.1:c.1274T>C
ENST00000639046.1:c.764T>C ENSP00000492659.1:p.Leu255Pro
ENST00000639111.2:c.1373T>C ENSP00000492125.2:p.Leu458Pro
ENST00000639213.2:c.1397T>C MANE Select ENSP00000491909.2:p.Leu466Pro
ENST00000639278.1:c.2060T>C ENSP00000491958.1:n.2060T>C
ENST00000639384.1:c.*1578T>C ENSP00000491240.1:n.*1578T>C
ENST00000639424.1:c.*597T>C ENSP00000491245.1:n.*597T>C
ENST00000639683.1:c.1331T>C ENSP00000492581.1:p.Leu444Pro
ENST00000639975.1:c.1307T>C ENSP00000492096.1:p.Leu436Pro
ENST00000640500.1:n.671T>C
ENST00000640739.1:n.6344T>C
ENST00000640910.1:c.835T>C
ENST00000640985.1:c.1310T>C ENSP00000492293.1:p.Leu437Pro
ENST00000641017.1:c.1466T>C ENSP00000493461.1:p.Leu489Pro
ENST00000356592.7:c.1397T>C ENSP00000349000.3:p.Leu466Pro
ENST00000361925.8:c.1373T>C ENSP00000354651.4:p.Leu458Pro
ENST00000414552.6:c.1517T>C ENSP00000410732.2:p.Leu506Pro
ENST00000522990.5:c.*975T>C ENSP00000430732.1:n.*975T>C
ENST00000523372.1:c.1494T>C ENSP00000430124.1:n.1494T>C
NM_000816.3:c.1373T>C NP_000807.2:p.Leu458Pro
NM_198903.2:c.1517T>C NP_944493.2:p.Leu506Pro
NM_198904.2:c.1397T>C NP_944494.1:p.Leu466Pro
NM_001375339.1:c.1388T>C NP_001362268.1:p.Leu463Pro
NM_001375340.1:c.*231T>C NP_001362269.1:n.*231T>C
NM_001375341.1:c.1394T>C NP_001362270.1:p.Leu465Pro
NM_001375342.1:c.1370T>C NP_001362271.1:p.Leu457Pro
NM_001375343.1:c.1493T>C NP_001362272.1:p.Leu498Pro
NM_001375344.1:c.1436T>C NP_001362273.1:p.Leu479Pro
NM_001375345.1:c.1307T>C NP_001362274.1:p.Leu436Pro
NM_001375346.1:c.1331T>C NP_001362275.1:p.Leu444Pro
NM_001375347.1:c.1310T>C NP_001362276.1:p.Leu437Pro
NM_001375348.1:c.953T>C NP_001362277.1:p.Leu318Pro
NM_001375349.1:c.1088T>C NP_001362278.1:p.Leu363Pro
NM_001375350.1:c.977T>C NP_001362279.1:p.Leu326Pro
NM_198904.3:c.1397T>C NP_944494.1:p.Leu466Pro
NM_198904.4:c.1397T>C MANE Select NP_944494.1:p.Leu466Pro