Canonical Allele Identifier: CA1083683756

Gene: GABRG2

Linked Data

• dbSNP Id: rs1753774890
• gnomAD v3: 5-162155212-CAA-C
• gnomAD v4: 5-162155212-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162155214_162155215del , CM000667.2:g.162155214_162155215del	GRCh38
NC_000005.9:g.161582220_161582221del , CM000667.1:g.161582220_161582221del	GRCh37
NC_000005.8:g.161514798_161514799del	NCBI36
NG_009290.1:g.92573_92574del

Transcript Alleles

HGVS	Amino-acid change
ENST00000356592.8:c.3275_3276del
ENST00000361925.9:c.*1846_*1847del	ENSP00000354651.5:n.*1846_*1847del
ENST00000638552.1:c.*1846_*1847del	ENSP00000491763.1:n.*1846_*1847del
ENST00000638660.1:c.*1846_*1847del	ENSP00000492869.1:n.*1846_*1847del
ENST00000638772.1:c.*5871_*5872del	ENSP00000491557.1:n.*5871_*5872del
ENST00000638877.1:c.3151_3152del
ENST00000639046.1:c.*1846_*1847del	ENSP00000492659.1:n.*1846_*1847del
ENST00000639111.2:c.*1846_*1847del	ENSP00000492125.2:n.*1846_*1847del
ENST00000639213.2:c.*1846_*1847del MANE Select	ENSP00000491909.2:n.*1846_*1847del
ENST00000639384.1:c.*3455_*3456del	ENSP00000491240.1:n.*3455_*3456del
ENST00000639683.1:c.*1846_*1847del	ENSP00000492581.1:n.*1846_*1847del
ENST00000639975.1:c.*1846_*1847del	ENSP00000492096.1:n.*1846_*1847del
ENST00000640500.1:n.2548_2549del
ENST00000640739.1:n.8221_8222del
ENST00000641017.1:c.3343_3344del	ENSP00000493461.1:n.3343_3344del
ENST00000356592.7:c.*1846_*1847del	ENSP00000349000.3:n.*1846_*1847del
ENST00000414552.6:c.*1846_*1847del	ENSP00000410732.2:n.*1846_*1847del
NM_000816.3:c.*1846_*1847del	NP_000807.2:n.*1846_*1847del
NM_198903.2:c.*1846_*1847del	NP_944493.2:n.*1846_*1847del
NM_198904.2:c.*1846_*1847del	NP_944494.1:n.*1846_*1847del
NM_001375339.1:c.*1846_*1847del	NP_001362268.1:n.*1846_*1847del
NM_001375340.1:c.*2108_*2109del	NP_001362269.1:n.*2108_*2109del
NM_001375341.1:c.*1846_*1847del	NP_001362270.1:n.*1846_*1847del
NM_001375342.1:c.*1846_*1847del	NP_001362271.1:n.*1846_*1847del
NM_001375343.1:c.*1846_*1847del	NP_001362272.1:n.*1846_*1847del
NM_001375344.1:c.*1846_*1847del	NP_001362273.1:n.*1846_*1847del
NM_001375345.1:c.*1846_*1847del	NP_001362274.1:n.*1846_*1847del
NM_001375346.1:c.*1846_*1847del	NP_001362275.1:n.*1846_*1847del
NM_001375347.1:c.*1846_*1847del	NP_001362276.1:n.*1846_*1847del
NM_001375348.1:c.*1846_*1847del	NP_001362277.1:n.*1846_*1847del
NM_001375349.1:c.*1846_*1847del	NP_001362278.1:n.*1846_*1847del
NM_001375350.1:c.*1846_*1847del	NP_001362279.1:n.*1846_*1847del
NM_198904.3:c.*1846_*1847del	NP_944494.1:n.*1846_*1847del
NM_198904.4:c.*1846_*1847del MANE Select	NP_944494.1:n.*1846_*1847del