Canonical Allele Identifier: CA362183682

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161580238A>G (hg19) ; chr5:g.162153232A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153232A>G , CM000667.2:g.162153232A>G	GRCh38
NC_000005.9:g.161580238A>G , CM000667.1:g.161580238A>G	GRCh37
NC_000005.8:g.161512816A>G	NCBI36
NG_009290.1:g.90591A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1293A>G
ENST00000361925.9:c.1388A>G	ENSP00000354651.5:p.Asp463Gly
ENST00000523372.2:c.1351A>G
ENST00000638253.1:n.546A>G
ENST00000638552.1:c.983A>G	ENSP00000491763.1:p.Asp328Gly
ENST00000638660.1:c.1007A>G	ENSP00000492869.1:p.Asp336Gly
ENST00000638772.1:c.*3889A>G	ENSP00000491557.1:n.*3889A>G
ENST00000638877.1:c.1169A>G
ENST00000639046.1:c.659A>G	ENSP00000492659.1:p.Asp220Gly
ENST00000639111.2:c.1268A>G	ENSP00000492125.2:p.Asp423Gly
ENST00000639213.2:c.1292A>G MANE Select	ENSP00000491909.2:p.Asp431Gly
ENST00000639278.1:c.1955A>G	ENSP00000491958.1:n.1955A>G
ENST00000639384.1:c.*1473A>G	ENSP00000491240.1:n.*1473A>G
ENST00000639424.1:c.*492A>G	ENSP00000491245.1:n.*492A>G
ENST00000639683.1:c.1226A>G	ENSP00000492581.1:p.Asp409Gly
ENST00000639975.1:c.1202A>G	ENSP00000492096.1:p.Asp401Gly
ENST00000640500.1:n.566A>G
ENST00000640739.1:n.6239A>G
ENST00000640910.1:c.730A>G
ENST00000640985.1:c.1205A>G	ENSP00000492293.1:p.Asp402Gly
ENST00000641017.1:c.1361A>G	ENSP00000493461.1:p.Asp454Gly
ENST00000356592.7:c.1292A>G	ENSP00000349000.3:p.Asp431Gly
ENST00000361925.8:c.1268A>G	ENSP00000354651.4:p.Asp423Gly
ENST00000414552.6:c.1412A>G	ENSP00000410732.2:p.Asp471Gly
ENST00000522990.5:c.*870A>G	ENSP00000430732.1:n.*870A>G
ENST00000523372.1:c.1389A>G	ENSP00000430124.1:n.1389A>G
NM_000816.3:c.1268A>G	NP_000807.2:p.Asp423Gly
NM_198903.2:c.1412A>G	NP_944493.2:p.Asp471Gly
NM_198904.2:c.1292A>G	NP_944494.1:p.Asp431Gly
NM_001375339.1:c.1283A>G	NP_001362268.1:p.Asp428Gly
NM_001375340.1:c.*126A>G	NP_001362269.1:n.*126A>G
NM_001375341.1:c.1289A>G	NP_001362270.1:p.Asp430Gly
NM_001375342.1:c.1265A>G	NP_001362271.1:p.Asp422Gly
NM_001375343.1:c.1388A>G	NP_001362272.1:p.Asp463Gly
NM_001375344.1:c.1331A>G	NP_001362273.1:p.Asp444Gly
NM_001375345.1:c.1202A>G	NP_001362274.1:p.Asp401Gly
NM_001375346.1:c.1226A>G	NP_001362275.1:p.Asp409Gly
NM_001375347.1:c.1205A>G	NP_001362276.1:p.Asp402Gly
NM_001375348.1:c.848A>G	NP_001362277.1:p.Asp283Gly
NM_001375349.1:c.983A>G	NP_001362278.1:p.Asp328Gly
NM_001375350.1:c.872A>G	NP_001362279.1:p.Asp291Gly
NM_198904.3:c.1292A>G	NP_944494.1:p.Asp431Gly
NM_198904.4:c.1292A>G MANE Select	NP_944494.1:p.Asp431Gly