Canonical Allele Identifier: CA362182341

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161576136G>C (hg19) ; chr5:g.162149130G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162149130G>C , CM000667.2:g.162149130G>C	GRCh38
NC_000005.9:g.161576136G>C , CM000667.1:g.161576136G>C	GRCh37
NC_000005.8:g.161508714G>C	NCBI36
NG_009290.1:g.86489G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.946G>C
ENST00000361925.9:c.1065G>C	ENSP00000354651.5:p.Met355Ile
ENST00000522053.2:n.836G>C
ENST00000523372.2:c.1028G>C
ENST00000638253.1:n.199G>C
ENST00000638552.1:c.660G>C	ENSP00000491763.1:p.Met220Ile
ENST00000638660.1:c.660G>C	ENSP00000492869.1:p.Met220Ile
ENST00000638772.1:c.945G>C	ENSP00000491557.1:p.Met315Ile
ENST00000638877.1:c.822G>C
ENST00000639046.1:c.336G>C	ENSP00000492659.1:p.Met112Ile
ENST00000639111.2:c.945G>C	ENSP00000492125.2:p.Met315Ile
ENST00000639213.2:c.945G>C MANE Select	ENSP00000491909.2:p.Met315Ile
ENST00000639278.1:c.873G>C	ENSP00000491958.1:p.Met291Ile
ENST00000639384.1:c.945G>C	ENSP00000491240.1:p.Met315Ile
ENST00000639424.1:c.*145G>C	ENSP00000491245.1:n.*145G>C
ENST00000639683.1:c.879G>C	ENSP00000492581.1:p.Met293Ile
ENST00000639975.1:c.879G>C	ENSP00000492096.1:p.Met293Ile
ENST00000640500.1:n.243G>C
ENST00000640574.1:c.660G>C	ENSP00000491582.1:p.Met220Ile
ENST00000640739.1:n.3476G>C
ENST00000640910.1:c.383G>C
ENST00000640985.1:c.858G>C	ENSP00000492293.1:p.Met286Ile
ENST00000641017.1:c.945G>C	ENSP00000493461.1:p.Met315Ile
ENST00000356592.7:c.945G>C	ENSP00000349000.3:p.Met315Ile
ENST00000361925.8:c.945G>C	ENSP00000354651.4:p.Met315Ile
ENST00000414552.6:c.1065G>C	ENSP00000410732.2:p.Met355Ile
ENST00000522053.1:c.660G>C	ENSP00000430182.1:p.Met220Ile
ENST00000522990.5:c.*547G>C	ENSP00000430732.1:n.*547G>C
ENST00000523372.1:c.1066G>C	ENSP00000430124.1:n.1066G>C
NM_000816.3:c.945G>C	NP_000807.2:p.Met315Ile
NM_198903.2:c.1065G>C	NP_944493.2:p.Met355Ile
NM_198904.2:c.945G>C	NP_944494.1:p.Met315Ile
NM_001375339.1:c.936G>C	NP_001362268.1:p.Met312Ile
NM_001375340.1:c.923-2600G>C	NP_001362269.1:n.923-2600G>C
NM_001375341.1:c.942G>C	NP_001362270.1:p.Met314Ile
NM_001375342.1:c.942G>C	NP_001362271.1:p.Met314Ile
NM_001375343.1:c.1065G>C	NP_001362272.1:p.Met355Ile
NM_001375344.1:c.984G>C	NP_001362273.1:p.Met328Ile
NM_001375345.1:c.879G>C	NP_001362274.1:p.Met293Ile
NM_001375346.1:c.879G>C	NP_001362275.1:p.Met293Ile
NM_001375347.1:c.858G>C	NP_001362276.1:p.Met286Ile
NM_001375348.1:c.525G>C	NP_001362277.1:p.Met175Ile
NM_001375349.1:c.660G>C	NP_001362278.1:p.Met220Ile
NM_001375350.1:c.525G>C	NP_001362279.1:p.Met175Ile
NM_198904.3:c.945G>C	NP_944494.1:p.Met315Ile
NM_198904.4:c.945G>C MANE Select	NP_944494.1:p.Met315Ile