Canonical Allele Identifier: CA447692041

Gene: GABRG2

Linked Data

• MyVariant Identifiers: chr5:g.161580359C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162153353C>A , CM000667.2:g.162153353C>A	GRCh38
NC_000005.9:g.161580359C>A , CM000667.1:g.161580359C>A	GRCh37
NC_000005.8:g.161512937C>A	NCBI36
NG_009290.1:g.90712C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356592.8:c.1414C>A
ENST00000361925.9:c.1509C>A	ENSP00000354651.5:p.Ser503=
ENST00000523372.2:c.1472C>A
ENST00000638253.1:n.667C>A
ENST00000638552.1:c.1104C>A	ENSP00000491763.1:p.Ser368=
ENST00000638660.1:c.1128C>A	ENSP00000492869.1:p.Ser376=
ENST00000638772.1:c.*4010C>A	ENSP00000491557.1:n.*4010C>A
ENST00000638877.1:c.1290C>A
ENST00000639046.1:c.780C>A	ENSP00000492659.1:p.Ser260=
ENST00000639111.2:c.1389C>A	ENSP00000492125.2:p.Ser463=
ENST00000639213.2:c.1413C>A MANE Select	ENSP00000491909.2:p.Ser471=
ENST00000639278.1:c.2076C>A	ENSP00000491958.1:n.2076C>A
ENST00000639384.1:c.*1594C>A	ENSP00000491240.1:n.*1594C>A
ENST00000639424.1:c.*613C>A	ENSP00000491245.1:n.*613C>A
ENST00000639683.1:c.1347C>A	ENSP00000492581.1:p.Ser449=
ENST00000639975.1:c.1323C>A	ENSP00000492096.1:p.Ser441=
ENST00000640500.1:n.687C>A
ENST00000640739.1:n.6360C>A
ENST00000640910.1:c.851C>A
ENST00000640985.1:c.1326C>A	ENSP00000492293.1:p.Ser442=
ENST00000641017.1:c.1482C>A	ENSP00000493461.1:p.Ser494=
ENST00000356592.7:c.1413C>A	ENSP00000349000.3:p.Ser471=
ENST00000361925.8:c.1389C>A	ENSP00000354651.4:p.Ser463=
ENST00000414552.6:c.1533C>A	ENSP00000410732.2:p.Ser511=
ENST00000522990.5:c.*991C>A	ENSP00000430732.1:n.*991C>A
ENST00000523372.1:c.1510C>A	ENSP00000430124.1:n.1510C>A
NM_000816.3:c.1389C>A	NP_000807.2:p.Ser463=
NM_198903.2:c.1533C>A	NP_944493.2:p.Ser511=
NM_198904.2:c.1413C>A	NP_944494.1:p.Ser471=
NM_001375339.1:c.1404C>A	NP_001362268.1:p.Ser468=
NM_001375340.1:c.*247C>A	NP_001362269.1:n.*247C>A
NM_001375341.1:c.1410C>A	NP_001362270.1:p.Ser470=
NM_001375342.1:c.1386C>A	NP_001362271.1:p.Ser462=
NM_001375343.1:c.1509C>A	NP_001362272.1:p.Ser503=
NM_001375344.1:c.1452C>A	NP_001362273.1:p.Ser484=
NM_001375345.1:c.1323C>A	NP_001362274.1:p.Ser441=
NM_001375346.1:c.1347C>A	NP_001362275.1:p.Ser449=
NM_001375347.1:c.1326C>A	NP_001362276.1:p.Ser442=
NM_001375348.1:c.969C>A	NP_001362277.1:p.Ser323=
NM_001375349.1:c.1104C>A	NP_001362278.1:p.Ser368=
NM_001375350.1:c.993C>A	NP_001362279.1:p.Ser331=
NM_198904.3:c.1413C>A	NP_944494.1:p.Ser471=
NM_198904.4:c.1413C>A MANE Select	NP_944494.1:p.Ser471=