Canonical Allele Identifier: CA362184177
Gene: GABRG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162153346G>T , CM000667.2:g.162153346G>T GRCh38
NC_000005.9:g.161580352G>T , CM000667.1:g.161580352G>T GRCh37
NC_000005.8:g.161512930G>T NCBI36
NG_009290.1:g.90705G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.1407G>T
ENST00000361925.9:c.1502G>T ENSP00000354651.5:p.Trp501Leu
ENST00000523372.2:c.1465G>T
ENST00000638253.1:n.660G>T
ENST00000638552.1:c.1097G>T ENSP00000491763.1:p.Trp366Leu
ENST00000638660.1:c.1121G>T ENSP00000492869.1:p.Trp374Leu
ENST00000638772.1:c.*4003G>T ENSP00000491557.1:n.*4003G>T
ENST00000638877.1:c.1283G>T
ENST00000639046.1:c.773G>T ENSP00000492659.1:p.Trp258Leu
ENST00000639111.2:c.1382G>T ENSP00000492125.2:p.Trp461Leu
ENST00000639213.2:c.1406G>T MANE Select ENSP00000491909.2:p.Trp469Leu
ENST00000639278.1:c.2069G>T ENSP00000491958.1:n.2069G>T
ENST00000639384.1:c.*1587G>T ENSP00000491240.1:n.*1587G>T
ENST00000639424.1:c.*606G>T ENSP00000491245.1:n.*606G>T
ENST00000639683.1:c.1340G>T ENSP00000492581.1:p.Trp447Leu
ENST00000639975.1:c.1316G>T ENSP00000492096.1:p.Trp439Leu
ENST00000640500.1:n.680G>T
ENST00000640739.1:n.6353G>T
ENST00000640910.1:c.844G>T
ENST00000640985.1:c.1319G>T ENSP00000492293.1:p.Trp440Leu
ENST00000641017.1:c.1475G>T ENSP00000493461.1:p.Trp492Leu
ENST00000356592.7:c.1406G>T ENSP00000349000.3:p.Trp469Leu
ENST00000361925.8:c.1382G>T ENSP00000354651.4:p.Trp461Leu
ENST00000414552.6:c.1526G>T ENSP00000410732.2:p.Trp509Leu
ENST00000522990.5:c.*984G>T ENSP00000430732.1:n.*984G>T
ENST00000523372.1:c.1503G>T ENSP00000430124.1:n.1503G>T
NM_000816.3:c.1382G>T NP_000807.2:p.Trp461Leu
NM_198903.2:c.1526G>T NP_944493.2:p.Trp509Leu
NM_198904.2:c.1406G>T NP_944494.1:p.Trp469Leu
NM_001375339.1:c.1397G>T NP_001362268.1:p.Trp466Leu
NM_001375340.1:c.*240G>T NP_001362269.1:n.*240G>T
NM_001375341.1:c.1403G>T NP_001362270.1:p.Trp468Leu
NM_001375342.1:c.1379G>T NP_001362271.1:p.Trp460Leu
NM_001375343.1:c.1502G>T NP_001362272.1:p.Trp501Leu
NM_001375344.1:c.1445G>T NP_001362273.1:p.Trp482Leu
NM_001375345.1:c.1316G>T NP_001362274.1:p.Trp439Leu
NM_001375346.1:c.1340G>T NP_001362275.1:p.Trp447Leu
NM_001375347.1:c.1319G>T NP_001362276.1:p.Trp440Leu
NM_001375348.1:c.962G>T NP_001362277.1:p.Trp321Leu
NM_001375349.1:c.1097G>T NP_001362278.1:p.Trp366Leu
NM_001375350.1:c.986G>T NP_001362279.1:p.Trp329Leu
NM_198904.3:c.1406G>T NP_944494.1:p.Trp469Leu
NM_198904.4:c.1406G>T MANE Select NP_944494.1:p.Trp469Leu