Canonical Allele Identifier: CA447691477

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161580104T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153098T>G , CM000667.2:g.162153098T>G	GRCh38
NC_000005.9:g.161580104T>G , CM000667.1:g.161580104T>G	GRCh37
NC_000005.8:g.161512682T>G	NCBI36
NG_009290.1:g.90457T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356592.8:c.1159T>G
ENST00000361925.9:c.1254T>G	ENSP00000354651.5:p.Pro418=
ENST00000523372.2:c.1217T>G
ENST00000638253.1:n.412T>G
ENST00000638552.1:c.849T>G	ENSP00000491763.1:p.Pro283=
ENST00000638660.1:c.873T>G	ENSP00000492869.1:p.Pro291=
ENST00000638772.1:c.*3755T>G	ENSP00000491557.1:n.*3755T>G
ENST00000638877.1:c.1035T>G
ENST00000639046.1:c.525T>G	ENSP00000492659.1:p.Pro175=
ENST00000639111.2:c.1134T>G	ENSP00000492125.2:p.Pro378=
ENST00000639213.2:c.1158T>G MANE Select	ENSP00000491909.2:p.Pro386=
ENST00000639278.1:c.1821T>G	ENSP00000491958.1:n.1821T>G
ENST00000639384.1:c.*1339T>G	ENSP00000491240.1:n.*1339T>G
ENST00000639424.1:c.*358T>G	ENSP00000491245.1:n.*358T>G
ENST00000639683.1:c.1092T>G	ENSP00000492581.1:p.Pro364=
ENST00000639975.1:c.1068T>G	ENSP00000492096.1:p.Pro356=
ENST00000640500.1:n.432T>G
ENST00000640739.1:n.6105T>G
ENST00000640910.1:c.596T>G
ENST00000640985.1:c.1071T>G	ENSP00000492293.1:p.Pro357=
ENST00000641017.1:c.1227T>G	ENSP00000493461.1:p.Pro409=
ENST00000356592.7:c.1158T>G	ENSP00000349000.3:p.Pro386=
ENST00000361925.8:c.1134T>G	ENSP00000354651.4:p.Pro378=
ENST00000414552.6:c.1278T>G	ENSP00000410732.2:p.Pro426=
ENST00000522990.5:c.*736T>G	ENSP00000430732.1:n.*736T>G
ENST00000523372.1:c.1255T>G	ENSP00000430124.1:n.1255T>G
NM_000816.3:c.1134T>G	NP_000807.2:p.Pro378=
NM_198903.2:c.1278T>G	NP_944493.2:p.Pro426=
NM_198904.2:c.1158T>G	NP_944494.1:p.Pro386=
NM_001375339.1:c.1149T>G	NP_001362268.1:p.Pro383=
NM_001375340.1:c.952T>G	NP_001362269.1:p.Tyr318Asp
NM_001375341.1:c.1155T>G	NP_001362270.1:p.Pro385=
NM_001375342.1:c.1131T>G	NP_001362271.1:p.Pro377=
NM_001375343.1:c.1254T>G	NP_001362272.1:p.Pro418=
NM_001375344.1:c.1197T>G	NP_001362273.1:p.Pro399=
NM_001375345.1:c.1068T>G	NP_001362274.1:p.Pro356=
NM_001375346.1:c.1092T>G	NP_001362275.1:p.Pro364=
NM_001375347.1:c.1071T>G	NP_001362276.1:p.Pro357=
NM_001375348.1:c.714T>G	NP_001362277.1:p.Pro238=
NM_001375349.1:c.849T>G	NP_001362278.1:p.Pro283=
NM_001375350.1:c.738T>G	NP_001362279.1:p.Pro246=
NM_198904.3:c.1158T>G	NP_944494.1:p.Pro386=
NM_198904.4:c.1158T>G MANE Select	NP_944494.1:p.Pro386=