Canonical Allele Identifier: CA1596382257
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162153336C= , CM000667.2:g.162153336C= GRCh38
NC_000005.9:g.161580342C= , CM000667.1:g.161580342C= GRCh37
NC_000005.8:g.161512920C= NCBI36
NG_009290.1:g.90695C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.1397C=
ENST00000361925.9:c.1492C= ENSP00000354651.5:p.Leu498=
ENST00000523372.2:c.1455C=
ENST00000638253.1:n.650C=
ENST00000638552.1:c.1087C= ENSP00000491763.1:p.Leu363=
ENST00000638660.1:c.1111C= ENSP00000492869.1:p.Leu371=
ENST00000638772.1:c.*3993C= ENSP00000491557.1:n.*3993C=
ENST00000638877.1:c.1273C=
ENST00000639046.1:c.763C= ENSP00000492659.1:p.Leu255=
ENST00000639111.2:c.1372C= ENSP00000492125.2:p.Leu458=
ENST00000639213.2:c.1396C= MANE Select ENSP00000491909.2:p.Leu466=
ENST00000639278.1:c.2059C= ENSP00000491958.1:n.2059C=
ENST00000639384.1:c.*1577C= ENSP00000491240.1:n.*1577C=
ENST00000639424.1:c.*596C= ENSP00000491245.1:n.*596C=
ENST00000639683.1:c.1330C= ENSP00000492581.1:p.Leu444=
ENST00000639975.1:c.1306C= ENSP00000492096.1:p.Leu436=
ENST00000640500.1:n.670C=
ENST00000640739.1:n.6343C=
ENST00000640910.1:c.834C=
ENST00000640985.1:c.1309C= ENSP00000492293.1:p.Leu437=
ENST00000641017.1:c.1465C= ENSP00000493461.1:p.Leu489=
ENST00000356592.7:c.1396C= ENSP00000349000.3:p.Leu466=
ENST00000361925.8:c.1372C= ENSP00000354651.4:p.Leu458=
ENST00000414552.6:c.1516C= ENSP00000410732.2:p.Leu506=
ENST00000522990.5:c.*974C= ENSP00000430732.1:n.*974C=
ENST00000523372.1:c.1493C= ENSP00000430124.1:n.1493C=
NM_000816.3:c.1372C= NP_000807.2:p.Leu458=
NM_198903.2:c.1516C= NP_944493.2:p.Leu506=
NM_198904.2:c.1396C= NP_944494.1:p.Leu466=
NM_001375339.1:c.1387C= NP_001362268.1:p.Leu463=
NM_001375340.1:c.*230C= NP_001362269.1:n.*230C=
NM_001375341.1:c.1393C= NP_001362270.1:p.Leu465=
NM_001375342.1:c.1369C= NP_001362271.1:p.Leu457=
NM_001375343.1:c.1492C= NP_001362272.1:p.Leu498=
NM_001375344.1:c.1435C= NP_001362273.1:p.Leu479=
NM_001375345.1:c.1306C= NP_001362274.1:p.Leu436=
NM_001375346.1:c.1330C= NP_001362275.1:p.Leu444=
NM_001375347.1:c.1309C= NP_001362276.1:p.Leu437=
NM_001375348.1:c.952C= NP_001362277.1:p.Leu318=
NM_001375349.1:c.1087C= NP_001362278.1:p.Leu363=
NM_001375350.1:c.976C= NP_001362279.1:p.Leu326=
NM_198904.3:c.1396C= NP_944494.1:p.Leu466=
NM_198904.4:c.1396C= MANE Select NP_944494.1:p.Leu466=