Canonical Allele Identifier: CA362182551

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161576233T>A (hg19) ; chr5:g.162149227T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162149227T>A , CM000667.2:g.162149227T>A	GRCh38
NC_000005.9:g.161576233T>A , CM000667.1:g.161576233T>A	GRCh37
NC_000005.8:g.161508811T>A	NCBI36
NG_009290.1:g.86586T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356592.8:c.1043T>A
ENST00000361925.9:c.1162T>A	ENSP00000354651.5:p.Ser388Thr
ENST00000523372.2:c.1125T>A
ENST00000638253.1:n.296T>A
ENST00000638552.1:c.757T>A	ENSP00000491763.1:p.Ser253Thr
ENST00000638660.1:c.757T>A	ENSP00000492869.1:p.Ser253Thr
ENST00000638772.1:c.1042T>A	ENSP00000491557.1:p.Ser348Thr
ENST00000638877.1:c.919T>A
ENST00000639046.1:c.433T>A	ENSP00000492659.1:p.Ser145Thr
ENST00000639111.2:c.1042T>A	ENSP00000492125.2:p.Ser348Thr
ENST00000639213.2:c.1042T>A MANE Select	ENSP00000491909.2:p.Ser348Thr
ENST00000639278.1:c.970T>A	ENSP00000491958.1:p.Ser324Thr
ENST00000639384.1:c.1042T>A	ENSP00000491240.1:p.Ser348Thr
ENST00000639424.1:c.*242T>A	ENSP00000491245.1:n.*242T>A
ENST00000639683.1:c.976T>A	ENSP00000492581.1:p.Ser326Thr
ENST00000639975.1:c.976T>A	ENSP00000492096.1:p.Ser326Thr
ENST00000640500.1:n.340T>A
ENST00000640574.1:c.757T>A	ENSP00000491582.1:p.Ser253Thr
ENST00000640739.1:n.3573T>A
ENST00000640910.1:c.480T>A
ENST00000640985.1:c.955T>A	ENSP00000492293.1:p.Ser319Thr
ENST00000641017.1:c.1042T>A	ENSP00000493461.1:p.Ser348Thr
ENST00000356592.7:c.1042T>A	ENSP00000349000.3:p.Ser348Thr
ENST00000361925.8:c.1042T>A	ENSP00000354651.4:p.Ser348Thr
ENST00000414552.6:c.1162T>A	ENSP00000410732.2:p.Ser388Thr
ENST00000522990.5:c.*644T>A	ENSP00000430732.1:n.*644T>A
ENST00000523372.1:c.1163T>A	ENSP00000430124.1:n.1163T>A
NM_000816.3:c.1042T>A	NP_000807.2:p.Ser348Thr
NM_198903.2:c.1162T>A	NP_944493.2:p.Ser388Thr
NM_198904.2:c.1042T>A	NP_944494.1:p.Ser348Thr
NM_001375339.1:c.1033T>A	NP_001362268.1:p.Ser345Thr
NM_001375340.1:c.923-2503T>A	NP_001362269.1:n.923-2503T>A
NM_001375341.1:c.1039T>A	NP_001362270.1:p.Ser347Thr
NM_001375342.1:c.1039T>A	NP_001362271.1:p.Ser347Thr
NM_001375343.1:c.1162T>A	NP_001362272.1:p.Ser388Thr
NM_001375344.1:c.1081T>A	NP_001362273.1:p.Ser361Thr
NM_001375345.1:c.976T>A	NP_001362274.1:p.Ser326Thr
NM_001375346.1:c.976T>A	NP_001362275.1:p.Ser326Thr
NM_001375347.1:c.955T>A	NP_001362276.1:p.Ser319Thr
NM_001375348.1:c.622T>A	NP_001362277.1:p.Ser208Thr
NM_001375349.1:c.757T>A	NP_001362278.1:p.Ser253Thr
NM_001375350.1:c.622T>A	NP_001362279.1:p.Ser208Thr
NM_198904.3:c.1042T>A	NP_944494.1:p.Ser348Thr
NM_198904.4:c.1042T>A MANE Select	NP_944494.1:p.Ser348Thr