Canonical Allele Identifier: CA1083683451

Gene: GABRG2

Linked Data

• dbSNP Id: rs1765517684
• gnomAD v3: 5-162153439-C-CTTAAATAATCCTCTA
• gnomAD v4: 5-162153439-C-CTTAAATAATCCTCTA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153441_162153455dup , CM000667.2:g.162153441_162153455dup	GRCh38
NC_000005.9:g.161580447_161580461dup , CM000667.1:g.161580447_161580461dup	GRCh37
NC_000005.8:g.161513025_161513039dup	NCBI36
NG_009290.1:g.90800_90814dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1502_1516dup
ENST00000361925.9:c.*73_*87dup	ENSP00000354651.5:n.*73_*87dup
ENST00000523372.2:c.1560_1574dup
ENST00000638253.1:n.755_769dup
ENST00000638552.1:c.*73_*87dup	ENSP00000491763.1:n.*73_*87dup
ENST00000638660.1:c.*73_*87dup	ENSP00000492869.1:n.*73_*87dup
ENST00000638772.1:c.*4098_*4112dup	ENSP00000491557.1:n.*4098_*4112dup
ENST00000638877.1:c.1378_1392dup
ENST00000639046.1:c.*73_*87dup	ENSP00000492659.1:n.*73_*87dup
ENST00000639111.2:c.*73_*87dup	ENSP00000492125.2:n.*73_*87dup
ENST00000639213.2:c.*73_*87dup MANE Select	ENSP00000491909.2:n.*73_*87dup
ENST00000639278.1:c.2164_2178dup	ENSP00000491958.1:n.2164_2178dup
ENST00000639384.1:c.*1682_*1696dup	ENSP00000491240.1:n.*1682_*1696dup
ENST00000639424.1:c.*701_*715dup	ENSP00000491245.1:n.*701_*715dup
ENST00000639683.1:c.*73_*87dup	ENSP00000492581.1:n.*73_*87dup
ENST00000639975.1:c.*73_*87dup	ENSP00000492096.1:n.*73_*87dup
ENST00000640500.1:n.775_789dup
ENST00000640739.1:n.6448_6462dup
ENST00000640985.1:c.*73_*87dup	ENSP00000492293.1:n.*73_*87dup
ENST00000641017.1:c.1570_1584dup	ENSP00000493461.1:n.1570_1584dup
ENST00000356592.7:c.*73_*87dup	ENSP00000349000.3:n.*73_*87dup
ENST00000361925.8:c.*73_*87dup	ENSP00000354651.4:n.*73_*87dup
ENST00000414552.6:c.*73_*87dup	ENSP00000410732.2:n.*73_*87dup
ENST00000522990.5:c.*1079_*1093dup	ENSP00000430732.1:n.*1079_*1093dup
ENST00000523372.1:c.1598_1612dup	ENSP00000430124.1:n.1598_1612dup
NM_000816.3:c.*73_*87dup	NP_000807.2:n.*73_*87dup
NM_198903.2:c.*73_*87dup	NP_944493.2:n.*73_*87dup
NM_198904.2:c.*73_*87dup	NP_944494.1:n.*73_*87dup
NM_001375339.1:c.*73_*87dup	NP_001362268.1:n.*73_*87dup
NM_001375340.1:c.*335_*349dup	NP_001362269.1:n.*335_*349dup
NM_001375341.1:c.*73_*87dup	NP_001362270.1:n.*73_*87dup
NM_001375342.1:c.*73_*87dup	NP_001362271.1:n.*73_*87dup
NM_001375343.1:c.*73_*87dup	NP_001362272.1:n.*73_*87dup
NM_001375344.1:c.*73_*87dup	NP_001362273.1:n.*73_*87dup
NM_001375345.1:c.*73_*87dup	NP_001362274.1:n.*73_*87dup
NM_001375346.1:c.*73_*87dup	NP_001362275.1:n.*73_*87dup
NM_001375347.1:c.*73_*87dup	NP_001362276.1:n.*73_*87dup
NM_001375348.1:c.*73_*87dup	NP_001362277.1:n.*73_*87dup
NM_001375349.1:c.*73_*87dup	NP_001362278.1:n.*73_*87dup
NM_001375350.1:c.*73_*87dup	NP_001362279.1:n.*73_*87dup
NM_198904.3:c.*73_*87dup	NP_944494.1:n.*73_*87dup
NM_198904.4:c.*73_*87dup MANE Select	NP_944494.1:n.*73_*87dup