Canonical Allele Identifier: CA2676331040

Gene: GABRG2

Linked Data

• gnomAD v4: 5-162153440-TTAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153444_162153447del , CM000667.2:g.162153444_162153447del	GRCh38
NC_000005.9:g.161580450_161580453del , CM000667.1:g.161580450_161580453del	GRCh37
NC_000005.8:g.161513028_161513031del	NCBI36
NG_009290.1:g.90803_90806del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1505_1508del
ENST00000361925.9:c.*76_*79del	ENSP00000354651.5:n.*76_*79del
ENST00000523372.2:c.1563_1566del
ENST00000638253.1:n.758_761del
ENST00000638552.1:c.*76_*79del	ENSP00000491763.1:n.*76_*79del
ENST00000638660.1:c.*76_*79del	ENSP00000492869.1:n.*76_*79del
ENST00000638772.1:c.*4101_*4104del	ENSP00000491557.1:n.*4101_*4104del
ENST00000638877.1:c.1381_1384del
ENST00000639046.1:c.*76_*79del	ENSP00000492659.1:n.*76_*79del
ENST00000639111.2:c.*76_*79del	ENSP00000492125.2:n.*76_*79del
ENST00000639213.2:c.*76_*79del MANE Select	ENSP00000491909.2:n.*76_*79del
ENST00000639278.1:c.2167_2170del	ENSP00000491958.1:n.2167_2170del
ENST00000639384.1:c.*1685_*1688del	ENSP00000491240.1:n.*1685_*1688del
ENST00000639424.1:c.*704_*707del	ENSP00000491245.1:n.*704_*707del
ENST00000639683.1:c.*76_*79del	ENSP00000492581.1:n.*76_*79del
ENST00000639975.1:c.*76_*79del	ENSP00000492096.1:n.*76_*79del
ENST00000640500.1:n.778_781del
ENST00000640739.1:n.6451_6454del
ENST00000640985.1:c.*76_*79del	ENSP00000492293.1:n.*76_*79del
ENST00000641017.1:c.1573_1576del	ENSP00000493461.1:n.1573_1576del
ENST00000356592.7:c.*76_*79del	ENSP00000349000.3:n.*76_*79del
ENST00000361925.8:c.*76_*79del	ENSP00000354651.4:n.*76_*79del
ENST00000414552.6:c.*76_*79del	ENSP00000410732.2:n.*76_*79del
ENST00000522990.5:c.*1082_*1085del	ENSP00000430732.1:n.*1082_*1085del
ENST00000523372.1:c.1601_1604del	ENSP00000430124.1:n.1601_1604del
NM_000816.3:c.*76_*79del	NP_000807.2:n.*76_*79del
NM_198903.2:c.*76_*79del	NP_944493.2:n.*76_*79del
NM_198904.2:c.*76_*79del	NP_944494.1:n.*76_*79del
NM_001375339.1:c.*76_*79del	NP_001362268.1:n.*76_*79del
NM_001375340.1:c.*338_*341del	NP_001362269.1:n.*338_*341del
NM_001375341.1:c.*76_*79del	NP_001362270.1:n.*76_*79del
NM_001375342.1:c.*76_*79del	NP_001362271.1:n.*76_*79del
NM_001375343.1:c.*76_*79del	NP_001362272.1:n.*76_*79del
NM_001375344.1:c.*76_*79del	NP_001362273.1:n.*76_*79del
NM_001375345.1:c.*76_*79del	NP_001362274.1:n.*76_*79del
NM_001375346.1:c.*76_*79del	NP_001362275.1:n.*76_*79del
NM_001375347.1:c.*76_*79del	NP_001362276.1:n.*76_*79del
NM_001375348.1:c.*76_*79del	NP_001362277.1:n.*76_*79del
NM_001375349.1:c.*76_*79del	NP_001362278.1:n.*76_*79del
NM_001375350.1:c.*76_*79del	NP_001362279.1:n.*76_*79del
NM_198904.3:c.*76_*79del	NP_944494.1:n.*76_*79del
NM_198904.4:c.*76_*79del MANE Select	NP_944494.1:n.*76_*79del