Canonical Allele Identifier: CA410693927
Gene: TXNRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19918950T>G , CM000684.2:g.19918950T>G GRCh38
NC_000022.10:g.19906473T>G , CM000684.1:g.19906473T>G GRCh37
NC_000022.9:g.18286473T>G NCBI36
NG_011835.1:g.27887A>C , LRG_417:g.27887A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000400521.7:c.284A>C MANE Select ENSP00000383365.1:p.Lys95Thr
ENST00000334363.14:c.284A>C ENSP00000334451.9:p.Lys95Thr
ENST00000400518.5:c.194A>C ENSP00000383362.1:p.Lys65Thr
ENST00000400519.6:c.281A>C ENSP00000383363.1:p.Lys94Thr
ENST00000400521.6:c.284A>C ENSP00000383365.1:p.Lys95Thr
ENST00000400525.6:c.215A>C ENSP00000383369.3:p.Lys72Thr
ENST00000474308.5:c.227A>C ENSP00000485665.1:p.Lys76Thr
ENST00000491939.6:c.188A>C ENSP00000485543.1:p.Lys63Thr
ENST00000496729.2:n.289A>C
ENST00000542719.6:c.-5A>C ENSP00000485128.2:n.-5A>C
NM_001282512.1:c.284A>C NP_001269441.1:p.Lys95Thr
NM_006440.4:c.284A>C NP_006431.2:p.Lys95Thr
NM_001282512.2:c.284A>C NP_001269441.1:p.Lys95Thr
NM_001352300.1:c.281A>C NP_001339229.1:p.Lys94Thr
NM_001352301.1:c.194A>C NP_001339230.1:p.Lys65Thr
NM_001352302.1:c.-5A>C NP_001339231.1:n.-5A>C
NM_001352303.1:c.188A>C NP_001339232.1:p.Lys63Thr
NR_147957.1:n.416A>C
NM_006440.5:c.284A>C MANE Select NP_006431.2:p.Lys95Thr
NM_001282512.3:c.284A>C NP_001269441.1:p.Lys95Thr
NM_001352300.2:c.281A>C NP_001339229.1:p.Lys94Thr
NR_147957.2:n.242A>C
NM_001352301.2:c.194A>C NP_001339230.1:p.Lys65Thr
NM_001352302.2:c.-5A>C NP_001339231.1:n.-5A>C
NM_001352303.2:c.188A>C NP_001339232.1:p.Lys63Thr