Canonical Allele Identifier: CA410686472
Gene: TXNRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19895448T>G , CM000684.2:g.19895448T>G GRCh38
NC_000022.10:g.19882971T>G , CM000684.1:g.19882971T>G GRCh37
NC_000022.9:g.18262971T>G NCBI36
NG_011835.1:g.51389A>C , LRG_417:g.51389A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000400521.7:c.908A>C MANE Select ENSP00000383365.1:p.Lys303Thr
ENST00000334363.14:c.908A>C ENSP00000334451.9:p.Lys303Thr
ENST00000400518.5:c.818A>C ENSP00000383362.1:p.Lys273Thr
ENST00000400519.6:c.905A>C ENSP00000383363.1:p.Lys302Thr
ENST00000400521.6:c.908A>C ENSP00000383365.1:p.Lys303Thr
ENST00000400525.6:c.839A>C ENSP00000383369.3:p.Lys280Thr
ENST00000474308.5:c.851A>C ENSP00000485665.1:p.Lys284Thr
ENST00000475995.3:c.405A>C
ENST00000491939.6:c.812A>C ENSP00000485543.1:p.Lys271Thr
ENST00000494454.5:n.982A>C
ENST00000542719.6:c.620A>C ENSP00000485128.2:p.Lys207Thr
ENST00000634537.1:c.137A>C ENSP00000489208.1:p.Lys46Thr
ENST00000635155.1:n.494A>C
NM_001282512.1:c.908A>C NP_001269441.1:p.Lys303Thr
NM_006440.4:c.908A>C NP_006431.2:p.Lys303Thr
NM_001282512.2:c.908A>C NP_001269441.1:p.Lys303Thr
NM_001352300.1:c.905A>C NP_001339229.1:p.Lys302Thr
NM_001352301.1:c.818A>C NP_001339230.1:p.Lys273Thr
NM_001352302.1:c.620A>C NP_001339231.1:p.Lys207Thr
NM_001352303.1:c.812A>C NP_001339232.1:p.Lys271Thr
NR_147957.1:n.1040A>C
NM_006440.5:c.908A>C MANE Select NP_006431.2:p.Lys303Thr
NM_001282512.3:c.908A>C NP_001269441.1:p.Lys303Thr
NM_001352300.2:c.905A>C NP_001339229.1:p.Lys302Thr
NR_147957.2:n.866A>C
NM_001352301.2:c.818A>C NP_001339230.1:p.Lys273Thr
NM_001352302.2:c.620A>C NP_001339231.1:p.Lys207Thr
NM_001352303.2:c.812A>C NP_001339232.1:p.Lys271Thr