Canonical Allele Identifier: CA3545013

Gene: GABRG2

Linked Data

• dbSNP Id: rs775151354
• ExAC: 5:161580421 G / GAGAGACTGAGAGTCTCACT
• gnomAD v2: 5-161580421-G-GAGAGACTGAGAGTCTCACT
• gnomAD v4: 5-162153415-G-GAGAGACTGAGAGTCTCACT
• MyVariant Identifiers: chr5:g.161580421_161580422insAGAGACTGAGAGTCTCACT (hg19) ; chr5:g.162153415_162153416insAGAGACTGAGAGTCTCACT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153415_162153416insAGAGACTGAGAGTCTCACT , CM000667.2:g.162153415_162153416insAGAGACTGAGAGTCTCACT	GRCh38
NC_000005.9:g.161580421_161580422insAGAGACTGAGAGTCTCACT , CM000667.1:g.161580421_161580422insAGAGACTGAGAGTCTCACT	GRCh37
NC_000005.8:g.161512999_161513000insAGAGACTGAGAGTCTCACT	NCBI36
NG_009290.1:g.90774_90775insAGAGACTGAGAGTCTCACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1476_1477insAGAGACTGAGAGTCTCACT
ENST00000361925.9:c.*47_*48insAGAGACTGAGAGTCTCACT	ENSP00000354651.5:n.*47_*48insAGAGACTGAGAGTCTCACT
ENST00000523372.2:c.1534_1535insAGAGACTGAGAGTCTCACT
ENST00000638253.1:n.729_730insAGAGACTGAGAGTCTCACT
ENST00000638552.1:c.*47_*48insAGAGACTGAGAGTCTCACT	ENSP00000491763.1:n.*47_*48insAGAGACTGAGAGTCTCACT
ENST00000638660.1:c.*47_*48insAGAGACTGAGAGTCTCACT	ENSP00000492869.1:n.*47_*48insAGAGACTGAGAGTCTCACT
ENST00000638772.1:c.*4072_*4073insAGAGACTGAGAGTCTCACT	ENSP00000491557.1:n.*4072_*4073insAGAGACTGAGAGTCTCACT
ENST00000638877.1:c.1352_1353insAGAGACTGAGAGTCTCACT
ENST00000639046.1:c.*47_*48insAGAGACTGAGAGTCTCACT	ENSP00000492659.1:n.*47_*48insAGAGACTGAGAGTCTCACT
ENST00000639111.2:c.*47_*48insAGAGACTGAGAGTCTCACT	ENSP00000492125.2:n.*47_*48insAGAGACTGAGAGTCTCACT
ENST00000639213.2:c.*47_*48insAGAGACTGAGAGTCTCACT MANE Select	ENSP00000491909.2:n.*47_*48insAGAGACTGAGAGTCTCACT
ENST00000639278.1:c.2138_2139insAGAGACTGAGAGTCTCACT	ENSP00000491958.1:n.2138_2139insAGAGACTGAGAGTCTCACT
ENST00000639384.1:c.*1656_*1657insAGAGACTGAGAGTCTCACT	ENSP00000491240.1:n.*1656_*1657insAGAGACTGAGAGTCTCACT
ENST00000639424.1:c.*675_*676insAGAGACTGAGAGTCTCACT	ENSP00000491245.1:n.*675_*676insAGAGACTGAGAGTCTCACT
ENST00000639683.1:c.*47_*48insAGAGACTGAGAGTCTCACT	ENSP00000492581.1:n.*47_*48insAGAGACTGAGAGTCTCACT
ENST00000639975.1:c.*47_*48insAGAGACTGAGAGTCTCACT	ENSP00000492096.1:n.*47_*48insAGAGACTGAGAGTCTCACT
ENST00000640500.1:n.749_750insAGAGACTGAGAGTCTCACT
ENST00000640739.1:n.6422_6423insAGAGACTGAGAGTCTCACT
ENST00000640910.1:c.913_914insAGAGACTGAGAGTCTCACT
ENST00000640985.1:c.*47_*48insAGAGACTGAGAGTCTCACT	ENSP00000492293.1:n.*47_*48insAGAGACTGAGAGTCTCACT
ENST00000641017.1:c.1544_1545insAGAGACTGAGAGTCTCACT	ENSP00000493461.1:n.1544_1545insAGAGACTGAGAGTCTCACT
ENST00000356592.7:c.*47_*48insAGAGACTGAGAGTCTCACT	ENSP00000349000.3:n.*47_*48insAGAGACTGAGAGTCTCACT
ENST00000361925.8:c.*47_*48insAGAGACTGAGAGTCTCACT	ENSP00000354651.4:n.*47_*48insAGAGACTGAGAGTCTCACT
ENST00000414552.6:c.*47_*48insAGAGACTGAGAGTCTCACT	ENSP00000410732.2:n.*47_*48insAGAGACTGAGAGTCTCACT
ENST00000522990.5:c.*1053_*1054insAGAGACTGAGAGTCTCACT	ENSP00000430732.1:n.*1053_*1054insAGAGACTGAGAGTCTCACT
ENST00000523372.1:c.1572_1573insAGAGACTGAGAGTCTCACT	ENSP00000430124.1:n.1572_1573insAGAGACTGAGAGTCTCACT
NM_000816.3:c.*47_*48insAGAGACTGAGAGTCTCACT	NP_000807.2:n.*47_*48insAGAGACTGAGAGTCTCACT
NM_198903.2:c.*47_*48insAGAGACTGAGAGTCTCACT	NP_944493.2:n.*47_*48insAGAGACTGAGAGTCTCACT
NM_198904.2:c.*47_*48insAGAGACTGAGAGTCTCACT	NP_944494.1:n.*47_*48insAGAGACTGAGAGTCTCACT
NM_001375339.1:c.*47_*48insAGAGACTGAGAGTCTCACT	NP_001362268.1:n.*47_*48insAGAGACTGAGAGTCTCACT
NM_001375340.1:c.*309_*310insAGAGACTGAGAGTCTCACT	NP_001362269.1:n.*309_*310insAGAGACTGAGAGTCTCACT
NM_001375341.1:c.*47_*48insAGAGACTGAGAGTCTCACT	NP_001362270.1:n.*47_*48insAGAGACTGAGAGTCTCACT
NM_001375342.1:c.*47_*48insAGAGACTGAGAGTCTCACT	NP_001362271.1:n.*47_*48insAGAGACTGAGAGTCTCACT
NM_001375343.1:c.*47_*48insAGAGACTGAGAGTCTCACT	NP_001362272.1:n.*47_*48insAGAGACTGAGAGTCTCACT
NM_001375344.1:c.*47_*48insAGAGACTGAGAGTCTCACT	NP_001362273.1:n.*47_*48insAGAGACTGAGAGTCTCACT
NM_001375345.1:c.*47_*48insAGAGACTGAGAGTCTCACT	NP_001362274.1:n.*47_*48insAGAGACTGAGAGTCTCACT
NM_001375346.1:c.*47_*48insAGAGACTGAGAGTCTCACT	NP_001362275.1:n.*47_*48insAGAGACTGAGAGTCTCACT
NM_001375347.1:c.*47_*48insAGAGACTGAGAGTCTCACT	NP_001362276.1:n.*47_*48insAGAGACTGAGAGTCTCACT
NM_001375348.1:c.*47_*48insAGAGACTGAGAGTCTCACT	NP_001362277.1:n.*47_*48insAGAGACTGAGAGTCTCACT
NM_001375349.1:c.*47_*48insAGAGACTGAGAGTCTCACT	NP_001362278.1:n.*47_*48insAGAGACTGAGAGTCTCACT
NM_001375350.1:c.*47_*48insAGAGACTGAGAGTCTCACT	NP_001362279.1:n.*47_*48insAGAGACTGAGAGTCTCACT
NM_198904.3:c.*47_*48insAGAGACTGAGAGTCTCACT	NP_944494.1:n.*47_*48insAGAGACTGAGAGTCTCACT
NM_198904.4:c.*47_*48insAGAGACTGAGAGTCTCACT MANE Select	NP_944494.1:n.*47_*48insAGAGACTGAGAGTCTCACT