Canonical Allele Identifier: CA362184094
Gene: GABRG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162153328T>A , CM000667.2:g.162153328T>A GRCh38
NC_000005.9:g.161580334T>A , CM000667.1:g.161580334T>A GRCh37
NC_000005.8:g.161512912T>A NCBI36
NG_009290.1:g.90687T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.1389T>A
ENST00000361925.9:c.1484T>A ENSP00000354651.5:p.Leu495Gln
ENST00000523372.2:c.1447T>A
ENST00000638253.1:n.642T>A
ENST00000638552.1:c.1079T>A ENSP00000491763.1:p.Leu360Gln
ENST00000638660.1:c.1103T>A ENSP00000492869.1:p.Leu368Gln
ENST00000638772.1:c.*3985T>A ENSP00000491557.1:n.*3985T>A
ENST00000638877.1:c.1265T>A
ENST00000639046.1:c.755T>A ENSP00000492659.1:p.Leu252Gln
ENST00000639111.2:c.1364T>A ENSP00000492125.2:p.Leu455Gln
ENST00000639213.2:c.1388T>A MANE Select ENSP00000491909.2:p.Leu463Gln
ENST00000639278.1:c.2051T>A ENSP00000491958.1:n.2051T>A
ENST00000639384.1:c.*1569T>A ENSP00000491240.1:n.*1569T>A
ENST00000639424.1:c.*588T>A ENSP00000491245.1:n.*588T>A
ENST00000639683.1:c.1322T>A ENSP00000492581.1:p.Leu441Gln
ENST00000639975.1:c.1298T>A ENSP00000492096.1:p.Leu433Gln
ENST00000640500.1:n.662T>A
ENST00000640739.1:n.6335T>A
ENST00000640910.1:c.826T>A
ENST00000640985.1:c.1301T>A ENSP00000492293.1:p.Leu434Gln
ENST00000641017.1:c.1457T>A ENSP00000493461.1:p.Leu486Gln
ENST00000356592.7:c.1388T>A ENSP00000349000.3:p.Leu463Gln
ENST00000361925.8:c.1364T>A ENSP00000354651.4:p.Leu455Gln
ENST00000414552.6:c.1508T>A ENSP00000410732.2:p.Leu503Gln
ENST00000522990.5:c.*966T>A ENSP00000430732.1:n.*966T>A
ENST00000523372.1:c.1485T>A ENSP00000430124.1:n.1485T>A
NM_000816.3:c.1364T>A NP_000807.2:p.Leu455Gln
NM_198903.2:c.1508T>A NP_944493.2:p.Leu503Gln
NM_198904.2:c.1388T>A NP_944494.1:p.Leu463Gln
NM_001375339.1:c.1379T>A NP_001362268.1:p.Leu460Gln
NM_001375340.1:c.*222T>A NP_001362269.1:n.*222T>A
NM_001375341.1:c.1385T>A NP_001362270.1:p.Leu462Gln
NM_001375342.1:c.1361T>A NP_001362271.1:p.Leu454Gln
NM_001375343.1:c.1484T>A NP_001362272.1:p.Leu495Gln
NM_001375344.1:c.1427T>A NP_001362273.1:p.Leu476Gln
NM_001375345.1:c.1298T>A NP_001362274.1:p.Leu433Gln
NM_001375346.1:c.1322T>A NP_001362275.1:p.Leu441Gln
NM_001375347.1:c.1301T>A NP_001362276.1:p.Leu434Gln
NM_001375348.1:c.944T>A NP_001362277.1:p.Leu315Gln
NM_001375349.1:c.1079T>A NP_001362278.1:p.Leu360Gln
NM_001375350.1:c.968T>A NP_001362279.1:p.Leu323Gln
NM_198904.3:c.1388T>A NP_944494.1:p.Leu463Gln
NM_198904.4:c.1388T>A MANE Select NP_944494.1:p.Leu463Gln