Canonical Allele Identifier: CA362182515

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161576218T>A (hg19) ; chr5:g.162149212T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162149212T>A , CM000667.2:g.162149212T>A	GRCh38
NC_000005.9:g.161576218T>A , CM000667.1:g.161576218T>A	GRCh37
NC_000005.8:g.161508796T>A	NCBI36
NG_009290.1:g.86571T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356592.8:c.1028T>A
ENST00000361925.9:c.1147T>A	ENSP00000354651.5:p.Phe383Ile
ENST00000523372.2:c.1110T>A
ENST00000638253.1:n.281T>A
ENST00000638552.1:c.742T>A	ENSP00000491763.1:p.Phe248Ile
ENST00000638660.1:c.742T>A	ENSP00000492869.1:p.Phe248Ile
ENST00000638772.1:c.1027T>A	ENSP00000491557.1:p.Phe343Ile
ENST00000638877.1:c.904T>A
ENST00000639046.1:c.418T>A	ENSP00000492659.1:p.Phe140Ile
ENST00000639111.2:c.1027T>A	ENSP00000492125.2:p.Phe343Ile
ENST00000639213.2:c.1027T>A MANE Select	ENSP00000491909.2:p.Phe343Ile
ENST00000639278.1:c.955T>A	ENSP00000491958.1:p.Phe319Ile
ENST00000639384.1:c.1027T>A	ENSP00000491240.1:p.Phe343Ile
ENST00000639424.1:c.*227T>A	ENSP00000491245.1:n.*227T>A
ENST00000639683.1:c.961T>A	ENSP00000492581.1:p.Phe321Ile
ENST00000639975.1:c.961T>A	ENSP00000492096.1:p.Phe321Ile
ENST00000640500.1:n.325T>A
ENST00000640574.1:c.742T>A	ENSP00000491582.1:p.Phe248Ile
ENST00000640739.1:n.3558T>A
ENST00000640910.1:c.465T>A
ENST00000640985.1:c.940T>A	ENSP00000492293.1:p.Phe314Ile
ENST00000641017.1:c.1027T>A	ENSP00000493461.1:p.Phe343Ile
ENST00000356592.7:c.1027T>A	ENSP00000349000.3:p.Phe343Ile
ENST00000361925.8:c.1027T>A	ENSP00000354651.4:p.Phe343Ile
ENST00000414552.6:c.1147T>A	ENSP00000410732.2:p.Phe383Ile
ENST00000522990.5:c.*629T>A	ENSP00000430732.1:n.*629T>A
ENST00000523372.1:c.1148T>A	ENSP00000430124.1:n.1148T>A
NM_000816.3:c.1027T>A	NP_000807.2:p.Phe343Ile
NM_198903.2:c.1147T>A	NP_944493.2:p.Phe383Ile
NM_198904.2:c.1027T>A	NP_944494.1:p.Phe343Ile
NM_001375339.1:c.1018T>A	NP_001362268.1:p.Phe340Ile
NM_001375340.1:c.923-2518T>A	NP_001362269.1:n.923-2518T>A
NM_001375341.1:c.1024T>A	NP_001362270.1:p.Phe342Ile
NM_001375342.1:c.1024T>A	NP_001362271.1:p.Phe342Ile
NM_001375343.1:c.1147T>A	NP_001362272.1:p.Phe383Ile
NM_001375344.1:c.1066T>A	NP_001362273.1:p.Phe356Ile
NM_001375345.1:c.961T>A	NP_001362274.1:p.Phe321Ile
NM_001375346.1:c.961T>A	NP_001362275.1:p.Phe321Ile
NM_001375347.1:c.940T>A	NP_001362276.1:p.Phe314Ile
NM_001375348.1:c.607T>A	NP_001362277.1:p.Phe203Ile
NM_001375349.1:c.742T>A	NP_001362278.1:p.Phe248Ile
NM_001375350.1:c.607T>A	NP_001362279.1:p.Phe203Ile
NM_198904.3:c.1027T>A	NP_944494.1:p.Phe343Ile
NM_198904.4:c.1027T>A MANE Select	NP_944494.1:p.Phe343Ile