Canonical Allele Identifier: CA1596381987

Gene: GABRG2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153143T= , CM000667.2:g.162153143T=	GRCh38
NC_000005.9:g.161580149T= , CM000667.1:g.161580149T=	GRCh37
NC_000005.8:g.161512727T=	NCBI36
NG_009290.1:g.90502T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1204T=
ENST00000361925.9:c.1299T=	ENSP00000354651.5:p.Asn433=
ENST00000523372.2:c.1262T=
ENST00000638253.1:n.457T=
ENST00000638552.1:c.894T=	ENSP00000491763.1:p.Asn298=
ENST00000638660.1:c.918T=	ENSP00000492869.1:p.Asn306=
ENST00000638772.1:c.*3800T=	ENSP00000491557.1:n.*3800T=
ENST00000638877.1:c.1080T=
ENST00000639046.1:c.570T=	ENSP00000492659.1:p.Asn190=
ENST00000639111.2:c.1179T=	ENSP00000492125.2:p.Asn393=
ENST00000639213.2:c.1203T= MANE Select	ENSP00000491909.2:p.Asn401=
ENST00000639278.1:c.1866T=	ENSP00000491958.1:n.1866T=
ENST00000639384.1:c.*1384T=	ENSP00000491240.1:n.*1384T=
ENST00000639424.1:c.*403T=	ENSP00000491245.1:n.*403T=
ENST00000639683.1:c.1137T=	ENSP00000492581.1:p.Asn379=
ENST00000639975.1:c.1113T=	ENSP00000492096.1:p.Asn371=
ENST00000640500.1:n.477T=
ENST00000640739.1:n.6150T=
ENST00000640910.1:c.641T=
ENST00000640985.1:c.1116T=	ENSP00000492293.1:p.Asn372=
ENST00000641017.1:c.1272T=	ENSP00000493461.1:p.Asn424=
ENST00000356592.7:c.1203T=	ENSP00000349000.3:p.Asn401=
ENST00000361925.8:c.1179T=	ENSP00000354651.4:p.Asn393=
ENST00000414552.6:c.1323T=	ENSP00000410732.2:p.Asn441=
ENST00000522990.5:c.*781T=	ENSP00000430732.1:n.*781T=
ENST00000523372.1:c.1300T=	ENSP00000430124.1:n.1300T=
NM_000816.3:c.1179T=	NP_000807.2:p.Asn393=
NM_198903.2:c.1323T=	NP_944493.2:p.Asn441=
NM_198904.2:c.1203T=	NP_944494.1:p.Asn401=
NM_001375339.1:c.1194T=	NP_001362268.1:p.Asn398=
NM_001375340.1:c.*37T=	NP_001362269.1:n.*37T=
NM_001375341.1:c.1200T=	NP_001362270.1:p.Asn400=
NM_001375342.1:c.1176T=	NP_001362271.1:p.Asn392=
NM_001375343.1:c.1299T=	NP_001362272.1:p.Asn433=
NM_001375344.1:c.1242T=	NP_001362273.1:p.Asn414=
NM_001375345.1:c.1113T=	NP_001362274.1:p.Asn371=
NM_001375346.1:c.1137T=	NP_001362275.1:p.Asn379=
NM_001375347.1:c.1116T=	NP_001362276.1:p.Asn372=
NM_001375348.1:c.759T=	NP_001362277.1:p.Asn253=
NM_001375349.1:c.894T=	NP_001362278.1:p.Asn298=
NM_001375350.1:c.783T=	NP_001362279.1:p.Asn261=
NM_198904.3:c.1203T=	NP_944494.1:p.Asn401=
NM_198904.4:c.1203T= MANE Select	NP_944494.1:p.Asn401=