Canonical Allele Identifier: CA1596382215
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162153299T= , CM000667.2:g.162153299T= GRCh38
NC_000005.9:g.161580305T= , CM000667.1:g.161580305T= GRCh37
NC_000005.8:g.161512883T= NCBI36
NG_009290.1:g.90658T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.1360T=
ENST00000361925.9:c.1455T= ENSP00000354651.5:p.Ala485=
ENST00000523372.2:c.1418T=
ENST00000638253.1:n.613T=
ENST00000638552.1:c.1050T= ENSP00000491763.1:p.Ala350=
ENST00000638660.1:c.1074T= ENSP00000492869.1:p.Ala358=
ENST00000638772.1:c.*3956T= ENSP00000491557.1:n.*3956T=
ENST00000638877.1:c.1236T=
ENST00000639046.1:c.726T= ENSP00000492659.1:p.Ala242=
ENST00000639111.2:c.1335T= ENSP00000492125.2:p.Ala445=
ENST00000639213.2:c.1359T= MANE Select ENSP00000491909.2:p.Ala453=
ENST00000639278.1:c.2022T= ENSP00000491958.1:n.2022T=
ENST00000639384.1:c.*1540T= ENSP00000491240.1:n.*1540T=
ENST00000639424.1:c.*559T= ENSP00000491245.1:n.*559T=
ENST00000639683.1:c.1293T= ENSP00000492581.1:p.Ala431=
ENST00000639975.1:c.1269T= ENSP00000492096.1:p.Ala423=
ENST00000640500.1:n.633T=
ENST00000640739.1:n.6306T=
ENST00000640910.1:c.797T=
ENST00000640985.1:c.1272T= ENSP00000492293.1:p.Ala424=
ENST00000641017.1:c.1428T= ENSP00000493461.1:p.Ala476=
ENST00000356592.7:c.1359T= ENSP00000349000.3:p.Ala453=
ENST00000361925.8:c.1335T= ENSP00000354651.4:p.Ala445=
ENST00000414552.6:c.1479T= ENSP00000410732.2:p.Ala493=
ENST00000522990.5:c.*937T= ENSP00000430732.1:n.*937T=
ENST00000523372.1:c.1456T= ENSP00000430124.1:n.1456T=
NM_000816.3:c.1335T= NP_000807.2:p.Ala445=
NM_198903.2:c.1479T= NP_944493.2:p.Ala493=
NM_198904.2:c.1359T= NP_944494.1:p.Ala453=
NM_001375339.1:c.1350T= NP_001362268.1:p.Ala450=
NM_001375340.1:c.*193T= NP_001362269.1:n.*193T=
NM_001375341.1:c.1356T= NP_001362270.1:p.Ala452=
NM_001375342.1:c.1332T= NP_001362271.1:p.Ala444=
NM_001375343.1:c.1455T= NP_001362272.1:p.Ala485=
NM_001375344.1:c.1398T= NP_001362273.1:p.Ala466=
NM_001375345.1:c.1269T= NP_001362274.1:p.Ala423=
NM_001375346.1:c.1293T= NP_001362275.1:p.Ala431=
NM_001375347.1:c.1272T= NP_001362276.1:p.Ala424=
NM_001375348.1:c.915T= NP_001362277.1:p.Ala305=
NM_001375349.1:c.1050T= NP_001362278.1:p.Ala350=
NM_001375350.1:c.939T= NP_001362279.1:p.Ala313=
NM_198904.3:c.1359T= NP_944494.1:p.Ala453=
NM_198904.4:c.1359T= MANE Select NP_944494.1:p.Ala453=