Canonical Allele Identifier: CA650531595

Gene: GABRG2

Linked Data

• COSMIC: COSN22021321

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153861_162153862insG , CM000667.2:g.162153861_162153862insG	GRCh38
NC_000005.9:g.161580867_161580868insG , CM000667.1:g.161580867_161580868insG	GRCh37
NC_000005.8:g.161513445_161513446insG	NCBI36
NG_009290.1:g.91220_91221insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1922_1923insG
ENST00000361925.9:c.*493_*494insG	ENSP00000354651.5:n.*493_*494insG
ENST00000638552.1:c.*493_*494insG	ENSP00000491763.1:n.*493_*494insG
ENST00000638660.1:c.*493_*494insG	ENSP00000492869.1:n.*493_*494insG
ENST00000638772.1:c.*4518_*4519insG	ENSP00000491557.1:n.*4518_*4519insG
ENST00000638877.1:c.1798_1799insG
ENST00000639046.1:c.*493_*494insG	ENSP00000492659.1:n.*493_*494insG
ENST00000639111.2:c.*493_*494insG	ENSP00000492125.2:n.*493_*494insG
ENST00000639213.2:c.*493_*494insG MANE Select	ENSP00000491909.2:n.*493_*494insG
ENST00000639278.1:c.2584_2585insG	ENSP00000491958.1:n.2584_2585insG
ENST00000639384.1:c.*2102_*2103insG	ENSP00000491240.1:n.*2102_*2103insG
ENST00000639424.1:c.*1121_*1122insG	ENSP00000491245.1:n.*1121_*1122insG
ENST00000639683.1:c.*493_*494insG	ENSP00000492581.1:n.*493_*494insG
ENST00000639975.1:c.*493_*494insG	ENSP00000492096.1:n.*493_*494insG
ENST00000640500.1:n.1195_1196insG
ENST00000640739.1:n.6868_6869insG
ENST00000640985.1:c.*493_*494insG	ENSP00000492293.1:n.*493_*494insG
ENST00000641017.1:c.1990_1991insG	ENSP00000493461.1:n.1990_1991insG
ENST00000356592.7:c.*493_*494insG	ENSP00000349000.3:n.*493_*494insG
ENST00000414552.6:c.*493_*494insG	ENSP00000410732.2:n.*493_*494insG
ENST00000522990.5:c.*1499_*1500insG	ENSP00000430732.1:n.*1499_*1500insG
NM_000816.3:c.*493_*494insG	NP_000807.2:n.*493_*494insG
NM_198903.2:c.*493_*494insG	NP_944493.2:n.*493_*494insG
NM_198904.2:c.*493_*494insG	NP_944494.1:n.*493_*494insG
NM_001375339.1:c.*493_*494insG	NP_001362268.1:n.*493_*494insG
NM_001375340.1:c.*755_*756insG	NP_001362269.1:n.*755_*756insG
NM_001375341.1:c.*493_*494insG	NP_001362270.1:n.*493_*494insG
NM_001375342.1:c.*493_*494insG	NP_001362271.1:n.*493_*494insG
NM_001375343.1:c.*493_*494insG	NP_001362272.1:n.*493_*494insG
NM_001375344.1:c.*493_*494insG	NP_001362273.1:n.*493_*494insG
NM_001375345.1:c.*493_*494insG	NP_001362274.1:n.*493_*494insG
NM_001375346.1:c.*493_*494insG	NP_001362275.1:n.*493_*494insG
NM_001375347.1:c.*493_*494insG	NP_001362276.1:n.*493_*494insG
NM_001375348.1:c.*493_*494insG	NP_001362277.1:n.*493_*494insG
NM_001375349.1:c.*493_*494insG	NP_001362278.1:n.*493_*494insG
NM_001375350.1:c.*493_*494insG	NP_001362279.1:n.*493_*494insG
NM_198904.3:c.*493_*494insG	NP_944494.1:n.*493_*494insG
NM_198904.4:c.*493_*494insG MANE Select	NP_944494.1:n.*493_*494insG