Canonical Allele Identifier: CA2676331041

Gene: GABRG2

Linked Data

• gnomAD v4: 5-162153442-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153442_162153443insG , CM000667.2:g.162153442_162153443insG	GRCh38
NC_000005.9:g.161580448_161580449insG , CM000667.1:g.161580448_161580449insG	GRCh37
NC_000005.8:g.161513026_161513027insG	NCBI36
NG_009290.1:g.90801_90802insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1503_1504insG
ENST00000361925.9:c.*74_*75insG	ENSP00000354651.5:n.*74_*75insG
ENST00000523372.2:c.1561_1562insG
ENST00000638253.1:n.756_757insG
ENST00000638552.1:c.*74_*75insG	ENSP00000491763.1:n.*74_*75insG
ENST00000638660.1:c.*74_*75insG	ENSP00000492869.1:n.*74_*75insG
ENST00000638772.1:c.*4099_*4100insG	ENSP00000491557.1:n.*4099_*4100insG
ENST00000638877.1:c.1379_1380insG
ENST00000639046.1:c.*74_*75insG	ENSP00000492659.1:n.*74_*75insG
ENST00000639111.2:c.*74_*75insG	ENSP00000492125.2:n.*74_*75insG
ENST00000639213.2:c.*74_*75insG MANE Select	ENSP00000491909.2:n.*74_*75insG
ENST00000639278.1:c.2165_2166insG	ENSP00000491958.1:n.2165_2166insG
ENST00000639384.1:c.*1683_*1684insG	ENSP00000491240.1:n.*1683_*1684insG
ENST00000639424.1:c.*702_*703insG	ENSP00000491245.1:n.*702_*703insG
ENST00000639683.1:c.*74_*75insG	ENSP00000492581.1:n.*74_*75insG
ENST00000639975.1:c.*74_*75insG	ENSP00000492096.1:n.*74_*75insG
ENST00000640500.1:n.776_777insG
ENST00000640739.1:n.6449_6450insG
ENST00000640985.1:c.*74_*75insG	ENSP00000492293.1:n.*74_*75insG
ENST00000641017.1:c.1571_1572insG	ENSP00000493461.1:n.1571_1572insG
ENST00000356592.7:c.*74_*75insG	ENSP00000349000.3:n.*74_*75insG
ENST00000361925.8:c.*74_*75insG	ENSP00000354651.4:n.*74_*75insG
ENST00000414552.6:c.*74_*75insG	ENSP00000410732.2:n.*74_*75insG
ENST00000522990.5:c.*1080_*1081insG	ENSP00000430732.1:n.*1080_*1081insG
ENST00000523372.1:c.1599_1600insG	ENSP00000430124.1:n.1599_1600insG
NM_000816.3:c.*74_*75insG	NP_000807.2:n.*74_*75insG
NM_198903.2:c.*74_*75insG	NP_944493.2:n.*74_*75insG
NM_198904.2:c.*74_*75insG	NP_944494.1:n.*74_*75insG
NM_001375339.1:c.*74_*75insG	NP_001362268.1:n.*74_*75insG
NM_001375340.1:c.*336_*337insG	NP_001362269.1:n.*336_*337insG
NM_001375341.1:c.*74_*75insG	NP_001362270.1:n.*74_*75insG
NM_001375342.1:c.*74_*75insG	NP_001362271.1:n.*74_*75insG
NM_001375343.1:c.*74_*75insG	NP_001362272.1:n.*74_*75insG
NM_001375344.1:c.*74_*75insG	NP_001362273.1:n.*74_*75insG
NM_001375345.1:c.*74_*75insG	NP_001362274.1:n.*74_*75insG
NM_001375346.1:c.*74_*75insG	NP_001362275.1:n.*74_*75insG
NM_001375347.1:c.*74_*75insG	NP_001362276.1:n.*74_*75insG
NM_001375348.1:c.*74_*75insG	NP_001362277.1:n.*74_*75insG
NM_001375349.1:c.*74_*75insG	NP_001362278.1:n.*74_*75insG
NM_001375350.1:c.*74_*75insG	NP_001362279.1:n.*74_*75insG
NM_198904.3:c.*74_*75insG	NP_944494.1:n.*74_*75insG
NM_198904.4:c.*74_*75insG MANE Select	NP_944494.1:n.*74_*75insG