Canonical Allele Identifier: CA362183934

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161580298C>A (hg19) ; chr5:g.162153292C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153292C>A , CM000667.2:g.162153292C>A	GRCh38
NC_000005.9:g.161580298C>A , CM000667.1:g.161580298C>A	GRCh37
NC_000005.8:g.161512876C>A	NCBI36
NG_009290.1:g.90651C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1353C>A
ENST00000361925.9:c.1448C>A	ENSP00000354651.5:p.Ser483Tyr
ENST00000523372.2:c.1411C>A
ENST00000638253.1:n.606C>A
ENST00000638552.1:c.1043C>A	ENSP00000491763.1:p.Ser348Tyr
ENST00000638660.1:c.1067C>A	ENSP00000492869.1:p.Ser356Tyr
ENST00000638772.1:c.*3949C>A	ENSP00000491557.1:n.*3949C>A
ENST00000638877.1:c.1229C>A
ENST00000639046.1:c.719C>A	ENSP00000492659.1:p.Ser240Tyr
ENST00000639111.2:c.1328C>A	ENSP00000492125.2:p.Ser443Tyr
ENST00000639213.2:c.1352C>A MANE Select	ENSP00000491909.2:p.Ser451Tyr
ENST00000639278.1:c.2015C>A	ENSP00000491958.1:n.2015C>A
ENST00000639384.1:c.*1533C>A	ENSP00000491240.1:n.*1533C>A
ENST00000639424.1:c.*552C>A	ENSP00000491245.1:n.*552C>A
ENST00000639683.1:c.1286C>A	ENSP00000492581.1:p.Ser429Tyr
ENST00000639975.1:c.1262C>A	ENSP00000492096.1:p.Ser421Tyr
ENST00000640500.1:n.626C>A
ENST00000640739.1:n.6299C>A
ENST00000640910.1:c.790C>A
ENST00000640985.1:c.1265C>A	ENSP00000492293.1:p.Ser422Tyr
ENST00000641017.1:c.1421C>A	ENSP00000493461.1:p.Ser474Tyr
ENST00000356592.7:c.1352C>A	ENSP00000349000.3:p.Ser451Tyr
ENST00000361925.8:c.1328C>A	ENSP00000354651.4:p.Ser443Tyr
ENST00000414552.6:c.1472C>A	ENSP00000410732.2:p.Ser491Tyr
ENST00000522990.5:c.*930C>A	ENSP00000430732.1:n.*930C>A
ENST00000523372.1:c.1449C>A	ENSP00000430124.1:n.1449C>A
NM_000816.3:c.1328C>A	NP_000807.2:p.Ser443Tyr
NM_198903.2:c.1472C>A	NP_944493.2:p.Ser491Tyr
NM_198904.2:c.1352C>A	NP_944494.1:p.Ser451Tyr
NM_001375339.1:c.1343C>A	NP_001362268.1:p.Ser448Tyr
NM_001375340.1:c.*186C>A	NP_001362269.1:n.*186C>A
NM_001375341.1:c.1349C>A	NP_001362270.1:p.Ser450Tyr
NM_001375342.1:c.1325C>A	NP_001362271.1:p.Ser442Tyr
NM_001375343.1:c.1448C>A	NP_001362272.1:p.Ser483Tyr
NM_001375344.1:c.1391C>A	NP_001362273.1:p.Ser464Tyr
NM_001375345.1:c.1262C>A	NP_001362274.1:p.Ser421Tyr
NM_001375346.1:c.1286C>A	NP_001362275.1:p.Ser429Tyr
NM_001375347.1:c.1265C>A	NP_001362276.1:p.Ser422Tyr
NM_001375348.1:c.908C>A	NP_001362277.1:p.Ser303Tyr
NM_001375349.1:c.1043C>A	NP_001362278.1:p.Ser348Tyr
NM_001375350.1:c.932C>A	NP_001362279.1:p.Ser311Tyr
NM_198904.3:c.1352C>A	NP_944494.1:p.Ser451Tyr
NM_198904.4:c.1352C>A MANE Select	NP_944494.1:p.Ser451Tyr