Canonical Allele Identifier: CA2512198593
Gene: TXNRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19918976_19918977insAGGGCTACCTTCTTACCCGCGTGGCCGAGGCGTTCGGCGGC , CM000684.2:g.19918976_19918977insAGGGCTACCTTCTTACCCGCGTGGCCGAGGCGTTCGGCGGC GRCh38
NC_000022.10:g.19906499_19906500insAGGGCTACCTTCTTACCCGCGTGGCCGAGGCGTTCGGCGGC , CM000684.1:g.19906499_19906500insAGGGCTACCTTCTTACCCGCGTGGCCGAGGCGTTCGGCGGC GRCh37
NC_000022.9:g.18286499_18286500insAGGGCTACCTTCTTACCCGCGTGGCCGAGGCGTTCGGCGGC NCBI36
NG_011835.1:g.27860_27861insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT , LRG_417:g.27860_27861insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000400521.7:c.257_258insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT MANE Select ENSP00000383365.1:p.Cys86TrpfsTer13
ENST00000334363.14:c.257_258insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT ENSP00000334451.9:p.Cys86TrpfsTer13
ENST00000400518.5:c.167_168insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT ENSP00000383362.1:p.Cys56TrpfsTer13
ENST00000400519.6:c.254_255insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT ENSP00000383363.1:p.Cys85TrpfsTer13
ENST00000400521.6:c.257_258insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT ENSP00000383365.1:p.Cys86TrpfsTer13
ENST00000400525.6:c.188_189insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT ENSP00000383369.3:p.Cys63TrpfsTer13
ENST00000474308.5:c.200_201insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT ENSP00000485665.1:p.Cys67TrpfsTer13
ENST00000491939.6:c.161_162insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT ENSP00000485543.1:p.Cys54TrpfsTer13
ENST00000496729.2:n.262_263insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT
ENST00000542719.6:c.-32_-31insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT ENSP00000485128.2:n.-32_-31insGCCGCCGAACGCCTCGGCCACGCGGGTAAGA...
NM_001282512.1:c.257_258insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT NP_001269441.1:p.Cys86TrpfsTer13
NM_006440.4:c.257_258insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT NP_006431.2:p.Cys86TrpfsTer13
NM_001282512.2:c.257_258insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT NP_001269441.1:p.Cys86TrpfsTer13
NM_001352300.1:c.254_255insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT NP_001339229.1:p.Cys85TrpfsTer13
NM_001352301.1:c.167_168insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT NP_001339230.1:p.Cys56TrpfsTer13
NM_001352302.1:c.-32_-31insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT NP_001339231.1:n.-32_-31insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGG...
NM_001352303.1:c.161_162insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT NP_001339232.1:p.Cys54TrpfsTer13
NR_147957.1:n.389_390insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT
NM_006440.5:c.257_258insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT MANE Select NP_006431.2:p.Cys86TrpfsTer13
NM_001282512.3:c.257_258insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT NP_001269441.1:p.Cys86TrpfsTer13
NM_001352300.2:c.254_255insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT NP_001339229.1:p.Cys85TrpfsTer13
NR_147957.2:n.215_216insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT
NM_001352301.2:c.167_168insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT NP_001339230.1:p.Cys56TrpfsTer13
NM_001352302.2:c.-32_-31insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT NP_001339231.1:n.-32_-31insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGG...
NM_001352303.2:c.161_162insGCCGCCGAACGCCTCGGCCACGCGGGTAAGAAGGTAGCCCT NP_001339232.1:p.Cys54TrpfsTer13