Canonical Allele Identifier: CA362182617

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161576264A>T (hg19) ; chr5:g.162149258A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162149258A>T , CM000667.2:g.162149258A>T	GRCh38
NC_000005.9:g.161576264A>T , CM000667.1:g.161576264A>T	GRCh37
NC_000005.8:g.161508842A>T	NCBI36
NG_009290.1:g.86617A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1074A>T
ENST00000361925.9:c.1193A>T	ENSP00000354651.5:p.Tyr398Phe
ENST00000523372.2:c.1156A>T
ENST00000638253.1:n.327A>T
ENST00000638552.1:c.788A>T	ENSP00000491763.1:p.Tyr263Phe
ENST00000638660.1:c.788A>T	ENSP00000492869.1:p.Tyr263Phe
ENST00000638772.1:c.1073A>T	ENSP00000491557.1:p.Tyr358Phe
ENST00000638877.1:c.950A>T
ENST00000639046.1:c.464A>T	ENSP00000492659.1:p.Tyr155Phe
ENST00000639111.2:c.1073A>T	ENSP00000492125.2:p.Tyr358Phe
ENST00000639213.2:c.1073A>T MANE Select	ENSP00000491909.2:p.Tyr358Phe
ENST00000639278.1:c.1001A>T	ENSP00000491958.1:p.Tyr334Phe
ENST00000639384.1:c.1073A>T	ENSP00000491240.1:p.Tyr358Phe
ENST00000639424.1:c.*273A>T	ENSP00000491245.1:n.*273A>T
ENST00000639683.1:c.1007A>T	ENSP00000492581.1:p.Tyr336Phe
ENST00000639975.1:c.1007A>T	ENSP00000492096.1:p.Tyr336Phe
ENST00000640500.1:n.371A>T
ENST00000640574.1:c.788A>T	ENSP00000491582.1:p.Tyr263Phe
ENST00000640739.1:n.3604A>T
ENST00000640910.1:c.511A>T
ENST00000640985.1:c.986A>T	ENSP00000492293.1:p.Tyr329Phe
ENST00000641017.1:c.1073A>T	ENSP00000493461.1:p.Tyr358Phe
ENST00000356592.7:c.1073A>T	ENSP00000349000.3:p.Tyr358Phe
ENST00000361925.8:c.1073A>T	ENSP00000354651.4:p.Tyr358Phe
ENST00000414552.6:c.1193A>T	ENSP00000410732.2:p.Tyr398Phe
ENST00000522990.5:c.*675A>T	ENSP00000430732.1:n.*675A>T
ENST00000523372.1:c.1194A>T	ENSP00000430124.1:n.1194A>T
NM_000816.3:c.1073A>T	NP_000807.2:p.Tyr358Phe
NM_198903.2:c.1193A>T	NP_944493.2:p.Tyr398Phe
NM_198904.2:c.1073A>T	NP_944494.1:p.Tyr358Phe
NM_001375339.1:c.1064A>T	NP_001362268.1:p.Tyr355Phe
NM_001375340.1:c.923-2472A>T	NP_001362269.1:n.923-2472A>T
NM_001375341.1:c.1070A>T	NP_001362270.1:p.Tyr357Phe
NM_001375342.1:c.1070A>T	NP_001362271.1:p.Tyr357Phe
NM_001375343.1:c.1193A>T	NP_001362272.1:p.Tyr398Phe
NM_001375344.1:c.1112A>T	NP_001362273.1:p.Tyr371Phe
NM_001375345.1:c.1007A>T	NP_001362274.1:p.Tyr336Phe
NM_001375346.1:c.1007A>T	NP_001362275.1:p.Tyr336Phe
NM_001375347.1:c.986A>T	NP_001362276.1:p.Tyr329Phe
NM_001375348.1:c.653A>T	NP_001362277.1:p.Tyr218Phe
NM_001375349.1:c.788A>T	NP_001362278.1:p.Tyr263Phe
NM_001375350.1:c.653A>T	NP_001362279.1:p.Tyr218Phe
NM_198904.3:c.1073A>T	NP_944494.1:p.Tyr358Phe
NM_198904.4:c.1073A>T MANE Select	NP_944494.1:p.Tyr358Phe