Canonical Allele Identifier: CA1596380297
Gene: GABRG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162149312C= , CM000667.2:g.162149312C= GRCh38
NC_000005.9:g.161576318C= , CM000667.1:g.161576318C= GRCh37
NC_000005.8:g.161508896C= NCBI36
NG_009290.1:g.86671C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356592.8:c.1128C=
ENST00000361925.9:c.1247C= ENSP00000354651.5:p.Pro416=
ENST00000523372.2:c.1210C=
ENST00000638253.1:n.381C=
ENST00000638552.1:c.842C= ENSP00000491763.1:p.Pro281=
ENST00000638660.1:c.842C= ENSP00000492869.1:p.Pro281=
ENST00000638772.1:c.1127C= ENSP00000491557.1:p.Pro376=
ENST00000638877.1:c.1004C=
ENST00000639046.1:c.518C= ENSP00000492659.1:p.Pro173=
ENST00000639111.2:c.1127C= ENSP00000492125.2:p.Pro376=
ENST00000639213.2:c.1127C= MANE Select ENSP00000491909.2:p.Pro376=
ENST00000639278.1:c.1055C= ENSP00000491958.1:p.Pro352=
ENST00000639384.1:c.1127C= ENSP00000491240.1:p.Pro376=
ENST00000639424.1:c.*327C= ENSP00000491245.1:n.*327C=
ENST00000639683.1:c.1061C= ENSP00000492581.1:p.Pro354=
ENST00000639975.1:c.1061C= ENSP00000492096.1:p.Pro354=
ENST00000640500.1:n.425C=
ENST00000640574.1:c.842C= ENSP00000491582.1:p.Pro281=
ENST00000640739.1:n.3658C=
ENST00000640910.1:c.565C=
ENST00000640985.1:c.1040C= ENSP00000492293.1:p.Pro347=
ENST00000641017.1:c.1127C= ENSP00000493461.1:p.Pro376=
ENST00000356592.7:c.1127C= ENSP00000349000.3:p.Pro376=
ENST00000361925.8:c.1127C= ENSP00000354651.4:p.Pro376=
ENST00000414552.6:c.1247C= ENSP00000410732.2:p.Pro416=
ENST00000522990.5:c.*729C= ENSP00000430732.1:n.*729C=
ENST00000523372.1:c.1248C= ENSP00000430124.1:n.1248C=
NM_000816.3:c.1127C= NP_000807.2:p.Pro376=
NM_198903.2:c.1247C= NP_944493.2:p.Pro416=
NM_198904.2:c.1127C= NP_944494.1:p.Pro376=
NM_001375339.1:c.1118C= NP_001362268.1:p.Pro373=
NM_001375340.1:c.923-2418C= NP_001362269.1:n.923-2418C=
NM_001375341.1:c.1124C= NP_001362270.1:p.Pro375=
NM_001375342.1:c.1124C= NP_001362271.1:p.Pro375=
NM_001375343.1:c.1247C= NP_001362272.1:p.Pro416=
NM_001375344.1:c.1166C= NP_001362273.1:p.Pro389=
NM_001375345.1:c.1061C= NP_001362274.1:p.Pro354=
NM_001375346.1:c.1061C= NP_001362275.1:p.Pro354=
NM_001375347.1:c.1040C= NP_001362276.1:p.Pro347=
NM_001375348.1:c.707C= NP_001362277.1:p.Pro236=
NM_001375349.1:c.842C= NP_001362278.1:p.Pro281=
NM_001375350.1:c.707C= NP_001362279.1:p.Pro236=
NM_198904.3:c.1127C= NP_944494.1:p.Pro376=
NM_198904.4:c.1127C= MANE Select NP_944494.1:p.Pro376=