Canonical Allele Identifier: CA447691835

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161580242T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153236T>C , CM000667.2:g.162153236T>C	GRCh38
NC_000005.9:g.161580242T>C , CM000667.1:g.161580242T>C	GRCh37
NC_000005.8:g.161512820T>C	NCBI36
NG_009290.1:g.90595T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1297T>C
ENST00000361925.9:c.1392T>C	ENSP00000354651.5:p.Cys464=
ENST00000523372.2:c.1355T>C
ENST00000638253.1:n.550T>C
ENST00000638552.1:c.987T>C	ENSP00000491763.1:p.Cys329=
ENST00000638660.1:c.1011T>C	ENSP00000492869.1:p.Cys337=
ENST00000638772.1:c.*3893T>C	ENSP00000491557.1:n.*3893T>C
ENST00000638877.1:c.1173T>C
ENST00000639046.1:c.663T>C	ENSP00000492659.1:p.Cys221=
ENST00000639111.2:c.1272T>C	ENSP00000492125.2:p.Cys424=
ENST00000639213.2:c.1296T>C MANE Select	ENSP00000491909.2:p.Cys432=
ENST00000639278.1:c.1959T>C	ENSP00000491958.1:n.1959T>C
ENST00000639384.1:c.*1477T>C	ENSP00000491240.1:n.*1477T>C
ENST00000639424.1:c.*496T>C	ENSP00000491245.1:n.*496T>C
ENST00000639683.1:c.1230T>C	ENSP00000492581.1:p.Cys410=
ENST00000639975.1:c.1206T>C	ENSP00000492096.1:p.Cys402=
ENST00000640500.1:n.570T>C
ENST00000640739.1:n.6243T>C
ENST00000640910.1:c.734T>C
ENST00000640985.1:c.1209T>C	ENSP00000492293.1:p.Cys403=
ENST00000641017.1:c.1365T>C	ENSP00000493461.1:p.Cys455=
ENST00000356592.7:c.1296T>C	ENSP00000349000.3:p.Cys432=
ENST00000361925.8:c.1272T>C	ENSP00000354651.4:p.Cys424=
ENST00000414552.6:c.1416T>C	ENSP00000410732.2:p.Cys472=
ENST00000522990.5:c.*874T>C	ENSP00000430732.1:n.*874T>C
ENST00000523372.1:c.1393T>C	ENSP00000430124.1:n.1393T>C
NM_000816.3:c.1272T>C	NP_000807.2:p.Cys424=
NM_198903.2:c.1416T>C	NP_944493.2:p.Cys472=
NM_198904.2:c.1296T>C	NP_944494.1:p.Cys432=
NM_001375339.1:c.1287T>C	NP_001362268.1:p.Cys429=
NM_001375340.1:c.*130T>C	NP_001362269.1:n.*130T>C
NM_001375341.1:c.1293T>C	NP_001362270.1:p.Cys431=
NM_001375342.1:c.1269T>C	NP_001362271.1:p.Cys423=
NM_001375343.1:c.1392T>C	NP_001362272.1:p.Cys464=
NM_001375344.1:c.1335T>C	NP_001362273.1:p.Cys445=
NM_001375345.1:c.1206T>C	NP_001362274.1:p.Cys402=
NM_001375346.1:c.1230T>C	NP_001362275.1:p.Cys410=
NM_001375347.1:c.1209T>C	NP_001362276.1:p.Cys403=
NM_001375348.1:c.852T>C	NP_001362277.1:p.Cys284=
NM_001375349.1:c.987T>C	NP_001362278.1:p.Cys329=
NM_001375350.1:c.876T>C	NP_001362279.1:p.Cys292=
NM_198904.3:c.1296T>C	NP_944494.1:p.Cys432=
NM_198904.4:c.1296T>C MANE Select	NP_944494.1:p.Cys432=