Canonical Allele Identifier: CA447691994

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161580326C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153320C>A , CM000667.2:g.162153320C>A	GRCh38
NC_000005.9:g.161580326C>A , CM000667.1:g.161580326C>A	GRCh37
NC_000005.8:g.161512904C>A	NCBI36
NG_009290.1:g.90679C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1381C>A
ENST00000361925.9:c.1476C>A	ENSP00000354651.5:p.Ala492=
ENST00000523372.2:c.1439C>A
ENST00000638253.1:n.634C>A
ENST00000638552.1:c.1071C>A	ENSP00000491763.1:p.Ala357=
ENST00000638660.1:c.1095C>A	ENSP00000492869.1:p.Ala365=
ENST00000638772.1:c.*3977C>A	ENSP00000491557.1:n.*3977C>A
ENST00000638877.1:c.1257C>A
ENST00000639046.1:c.747C>A	ENSP00000492659.1:p.Ala249=
ENST00000639111.2:c.1356C>A	ENSP00000492125.2:p.Ala452=
ENST00000639213.2:c.1380C>A MANE Select	ENSP00000491909.2:p.Ala460=
ENST00000639278.1:c.2043C>A	ENSP00000491958.1:n.2043C>A
ENST00000639384.1:c.*1561C>A	ENSP00000491240.1:n.*1561C>A
ENST00000639424.1:c.*580C>A	ENSP00000491245.1:n.*580C>A
ENST00000639683.1:c.1314C>A	ENSP00000492581.1:p.Ala438=
ENST00000639975.1:c.1290C>A	ENSP00000492096.1:p.Ala430=
ENST00000640500.1:n.654C>A
ENST00000640739.1:n.6327C>A
ENST00000640910.1:c.818C>A
ENST00000640985.1:c.1293C>A	ENSP00000492293.1:p.Ala431=
ENST00000641017.1:c.1449C>A	ENSP00000493461.1:p.Ala483=
ENST00000356592.7:c.1380C>A	ENSP00000349000.3:p.Ala460=
ENST00000361925.8:c.1356C>A	ENSP00000354651.4:p.Ala452=
ENST00000414552.6:c.1500C>A	ENSP00000410732.2:p.Ala500=
ENST00000522990.5:c.*958C>A	ENSP00000430732.1:n.*958C>A
ENST00000523372.1:c.1477C>A	ENSP00000430124.1:n.1477C>A
NM_000816.3:c.1356C>A	NP_000807.2:p.Ala452=
NM_198903.2:c.1500C>A	NP_944493.2:p.Ala500=
NM_198904.2:c.1380C>A	NP_944494.1:p.Ala460=
NM_001375339.1:c.1371C>A	NP_001362268.1:p.Ala457=
NM_001375340.1:c.*214C>A	NP_001362269.1:n.*214C>A
NM_001375341.1:c.1377C>A	NP_001362270.1:p.Ala459=
NM_001375342.1:c.1353C>A	NP_001362271.1:p.Ala451=
NM_001375343.1:c.1476C>A	NP_001362272.1:p.Ala492=
NM_001375344.1:c.1419C>A	NP_001362273.1:p.Ala473=
NM_001375345.1:c.1290C>A	NP_001362274.1:p.Ala430=
NM_001375346.1:c.1314C>A	NP_001362275.1:p.Ala438=
NM_001375347.1:c.1293C>A	NP_001362276.1:p.Ala431=
NM_001375348.1:c.936C>A	NP_001362277.1:p.Ala312=
NM_001375349.1:c.1071C>A	NP_001362278.1:p.Ala357=
NM_001375350.1:c.960C>A	NP_001362279.1:p.Ala320=
NM_198904.3:c.1380C>A	NP_944494.1:p.Ala460=
NM_198904.4:c.1380C>A MANE Select	NP_944494.1:p.Ala460=