Canonical Allele Identifier: CA362183920

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161580295A>T (hg19) ; chr5:g.162153289A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153289A>T , CM000667.2:g.162153289A>T	GRCh38
NC_000005.9:g.161580295A>T , CM000667.1:g.161580295A>T	GRCh37
NC_000005.8:g.161512873A>T	NCBI36
NG_009290.1:g.90648A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1350A>T
ENST00000361925.9:c.1445A>T	ENSP00000354651.5:p.Asp482Val
ENST00000523372.2:c.1408A>T
ENST00000638253.1:n.603A>T
ENST00000638552.1:c.1040A>T	ENSP00000491763.1:p.Asp347Val
ENST00000638660.1:c.1064A>T	ENSP00000492869.1:p.Asp355Val
ENST00000638772.1:c.*3946A>T	ENSP00000491557.1:n.*3946A>T
ENST00000638877.1:c.1226A>T
ENST00000639046.1:c.716A>T	ENSP00000492659.1:p.Asp239Val
ENST00000639111.2:c.1325A>T	ENSP00000492125.2:p.Asp442Val
ENST00000639213.2:c.1349A>T MANE Select	ENSP00000491909.2:p.Asp450Val
ENST00000639278.1:c.2012A>T	ENSP00000491958.1:n.2012A>T
ENST00000639384.1:c.*1530A>T	ENSP00000491240.1:n.*1530A>T
ENST00000639424.1:c.*549A>T	ENSP00000491245.1:n.*549A>T
ENST00000639683.1:c.1283A>T	ENSP00000492581.1:p.Asp428Val
ENST00000639975.1:c.1259A>T	ENSP00000492096.1:p.Asp420Val
ENST00000640500.1:n.623A>T
ENST00000640739.1:n.6296A>T
ENST00000640910.1:c.787A>T
ENST00000640985.1:c.1262A>T	ENSP00000492293.1:p.Asp421Val
ENST00000641017.1:c.1418A>T	ENSP00000493461.1:p.Asp473Val
ENST00000356592.7:c.1349A>T	ENSP00000349000.3:p.Asp450Val
ENST00000361925.8:c.1325A>T	ENSP00000354651.4:p.Asp442Val
ENST00000414552.6:c.1469A>T	ENSP00000410732.2:p.Asp490Val
ENST00000522990.5:c.*927A>T	ENSP00000430732.1:n.*927A>T
ENST00000523372.1:c.1446A>T	ENSP00000430124.1:n.1446A>T
NM_000816.3:c.1325A>T	NP_000807.2:p.Asp442Val
NM_198903.2:c.1469A>T	NP_944493.2:p.Asp490Val
NM_198904.2:c.1349A>T	NP_944494.1:p.Asp450Val
NM_001375339.1:c.1340A>T	NP_001362268.1:p.Asp447Val
NM_001375340.1:c.*183A>T	NP_001362269.1:n.*183A>T
NM_001375341.1:c.1346A>T	NP_001362270.1:p.Asp449Val
NM_001375342.1:c.1322A>T	NP_001362271.1:p.Asp441Val
NM_001375343.1:c.1445A>T	NP_001362272.1:p.Asp482Val
NM_001375344.1:c.1388A>T	NP_001362273.1:p.Asp463Val
NM_001375345.1:c.1259A>T	NP_001362274.1:p.Asp420Val
NM_001375346.1:c.1283A>T	NP_001362275.1:p.Asp428Val
NM_001375347.1:c.1262A>T	NP_001362276.1:p.Asp421Val
NM_001375348.1:c.905A>T	NP_001362277.1:p.Asp302Val
NM_001375349.1:c.1040A>T	NP_001362278.1:p.Asp347Val
NM_001375350.1:c.929A>T	NP_001362279.1:p.Asp310Val
NM_198904.3:c.1349A>T	NP_944494.1:p.Asp450Val
NM_198904.4:c.1349A>T MANE Select	NP_944494.1:p.Asp450Val