Canonical Allele Identifier: CA410693724
Gene: TXNRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19918891A>T , CM000684.2:g.19918891A>T GRCh38
NC_000022.10:g.19906414A>T , CM000684.1:g.19906414A>T GRCh37
NC_000022.9:g.18286414A>T NCBI36
NG_011835.1:g.27946T>A , LRG_417:g.27946T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000400521.7:c.343T>A MANE Select ENSP00000383365.1:p.Trp115Arg
ENST00000334363.14:c.343T>A ENSP00000334451.9:p.Trp115Arg
ENST00000400518.5:c.253T>A ENSP00000383362.1:p.Trp85Arg
ENST00000400519.6:c.340T>A ENSP00000383363.1:p.Trp114Arg
ENST00000400521.6:c.343T>A ENSP00000383365.1:p.Trp115Arg
ENST00000400525.6:c.274T>A ENSP00000383369.3:p.Trp92Arg
ENST00000474308.5:c.286T>A ENSP00000485665.1:p.Trp96Arg
ENST00000491939.6:c.247T>A ENSP00000485543.1:p.Trp83Arg
ENST00000496729.2:n.348T>A
ENST00000542719.6:c.55T>A ENSP00000485128.2:p.Trp19Arg
NM_001282512.1:c.343T>A NP_001269441.1:p.Trp115Arg
NM_006440.4:c.343T>A NP_006431.2:p.Trp115Arg
NM_001282512.2:c.343T>A NP_001269441.1:p.Trp115Arg
NM_001352300.1:c.340T>A NP_001339229.1:p.Trp114Arg
NM_001352301.1:c.253T>A NP_001339230.1:p.Trp85Arg
NM_001352302.1:c.55T>A NP_001339231.1:p.Trp19Arg
NM_001352303.1:c.247T>A NP_001339232.1:p.Trp83Arg
NR_147957.1:n.475T>A
NM_006440.5:c.343T>A MANE Select NP_006431.2:p.Trp115Arg
NM_001282512.3:c.343T>A NP_001269441.1:p.Trp115Arg
NM_001352300.2:c.340T>A NP_001339229.1:p.Trp114Arg
NR_147957.2:n.301T>A
NM_001352301.2:c.253T>A NP_001339230.1:p.Trp85Arg
NM_001352302.2:c.55T>A NP_001339231.1:p.Trp19Arg
NM_001352303.2:c.247T>A NP_001339232.1:p.Trp83Arg