Canonical Allele Identifier: CA2818401272
Gene: TXNRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19918994_19918995insAGCTGCGCAGCCCGGATGGCGGCGATGTAGCCG , CM000684.2:g.19918994_19918995insAGCTGCGCAGCCCGGATGGCGGCGATGTAGCCG GRCh38
NC_000022.10:g.19906517_19906518insAGCTGCGCAGCCCGGATGGCGGCGATGTAGCCG , CM000684.1:g.19906517_19906518insAGCTGCGCAGCCCGGATGGCGGCGATGTAGCCG GRCh37
NC_000022.9:g.18286517_18286518insAGCTGCGCAGCCCGGATGGCGGCGATGTAGCCG NCBI36
NG_011835.1:g.27842_27843insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT , LRG_417:g.27842_27843insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000400521.7:c.239_240insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT MANE Select ENSP00000383365.1:p.Trp80delinsCysGlyTyrIleAlaAlaIleArgAlaAla...
ENST00000334363.14:c.239_240insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT ENSP00000334451.9:p.Trp80delinsCysGlyTyrIleAlaAlaIleArgAlaAla...
ENST00000400518.5:c.149_150insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT ENSP00000383362.1:p.Trp50delinsCysGlyTyrIleAlaAlaIleArgAlaAla...
ENST00000400519.6:c.236_237insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT ENSP00000383363.1:p.Trp79delinsCysGlyTyrIleAlaAlaIleArgAlaAla...
ENST00000400521.6:c.239_240insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT ENSP00000383365.1:p.Trp80delinsCysGlyTyrIleAlaAlaIleArgAlaAla...
ENST00000400525.6:c.170_171insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT ENSP00000383369.3:p.Trp57delinsCysGlyTyrIleAlaAlaIleArgAlaAla...
ENST00000474308.5:c.182_183insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT ENSP00000485665.1:p.Trp61delinsCysGlyTyrIleAlaAlaIleArgAlaAla...
ENST00000491939.6:c.143_144insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT ENSP00000485543.1:p.Trp48delinsCysGlyTyrIleAlaAlaIleArgAlaAla...
ENST00000496729.2:n.244_245insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT
ENST00000542719.6:c.-50_-49insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT ENSP00000485128.2:n.-50_-49insCGGCTACATCGCCGCCATCCGGGCTGCGCAG...
NM_001282512.1:c.239_240insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT NP_001269441.1:p.Trp80delinsCysGlyTyrIleAlaAlaIleArgAlaAlaGln...
NM_006440.4:c.239_240insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT NP_006431.2:p.Trp80delinsCysGlyTyrIleAlaAlaIleArgAlaAlaGlnLeu...
NM_001282512.2:c.239_240insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT NP_001269441.1:p.Trp80delinsCysGlyTyrIleAlaAlaIleArgAlaAlaGln...
NM_001352300.1:c.236_237insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT NP_001339229.1:p.Trp79delinsCysGlyTyrIleAlaAlaIleArgAlaAlaGln...
NM_001352301.1:c.149_150insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT NP_001339230.1:p.Trp50delinsCysGlyTyrIleAlaAlaIleArgAlaAlaGln...
NM_001352302.1:c.-50_-49insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT NP_001339231.1:n.-50_-49insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT
NM_001352303.1:c.143_144insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT NP_001339232.1:p.Trp48delinsCysGlyTyrIleAlaAlaIleArgAlaAlaGln...
NR_147957.1:n.371_372insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT
NM_006440.5:c.239_240insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT MANE Select NP_006431.2:p.Trp80delinsCysGlyTyrIleAlaAlaIleArgAlaAlaGlnLeu...
NM_001282512.3:c.239_240insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT NP_001269441.1:p.Trp80delinsCysGlyTyrIleAlaAlaIleArgAlaAlaGln...
NM_001352300.2:c.236_237insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT NP_001339229.1:p.Trp79delinsCysGlyTyrIleAlaAlaIleArgAlaAlaGln...
NR_147957.2:n.197_198insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT
NM_001352301.2:c.149_150insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT NP_001339230.1:p.Trp50delinsCysGlyTyrIleAlaAlaIleArgAlaAlaGln...
NM_001352302.2:c.-50_-49insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT NP_001339231.1:n.-50_-49insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT
NM_001352303.2:c.143_144insCGGCTACATCGCCGCCATCCGGGCTGCGCAGCT NP_001339232.1:p.Trp48delinsCysGlyTyrIleAlaAlaIleArgAlaAlaGln...