Canonical Allele Identifier: CA410682034
Gene: TXNRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19880701G>T , CM000684.2:g.19880701G>T GRCh38
NC_000022.10:g.19868224G>T , CM000684.1:g.19868224G>T GRCh37
NC_000022.9:g.18248224G>T NCBI36
NG_011835.1:g.66136C>A , LRG_417:g.66136C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000400521.7:c.1103C>A MANE Select ENSP00000383365.1:p.Thr368Lys
ENST00000400518.5:c.1013C>A ENSP00000383362.1:p.Thr338Lys
ENST00000400519.6:c.1100C>A ENSP00000383363.1:p.Thr367Lys
ENST00000400521.6:c.1103C>A ENSP00000383365.1:p.Thr368Lys
ENST00000400525.6:c.1034C>A ENSP00000383369.3:p.Thr345Lys
ENST00000462330.5:c.26C>A ENSP00000485603.2:p.Thr9Lys
ENST00000462843.2:c.53C>A ENSP00000485466.2:p.Thr18Lys
ENST00000474308.5:c.1046C>A ENSP00000485665.1:p.Thr349Lys
ENST00000485358.5:c.71C>A ENSP00000485499.2:p.Thr24Lys
ENST00000487165.5:n.1197C>A
ENST00000494454.5:n.1177C>A
ENST00000495655.2:n.647C>A
ENST00000542719.6:c.815C>A ENSP00000485128.2:p.Thr272Lys
ENST00000634471.1:n.244-430C>A
ENST00000634537.1:c.332C>A ENSP00000489208.1:p.Thr111Lys
NM_006440.4:c.1103C>A NP_006431.2:p.Thr368Lys
NM_001352300.1:c.1100C>A NP_001339229.1:p.Thr367Lys
NM_001352301.1:c.1013C>A NP_001339230.1:p.Thr338Lys
NM_001352302.1:c.815C>A NP_001339231.1:p.Thr272Lys
NR_147957.1:n.1235C>A
NM_006440.5:c.1103C>A MANE Select NP_006431.2:p.Thr368Lys
NM_001352300.2:c.1100C>A NP_001339229.1:p.Thr367Lys
NR_147957.2:n.1061C>A
NM_001352301.2:c.1013C>A NP_001339230.1:p.Thr338Lys
NM_001352302.2:c.815C>A NP_001339231.1:p.Thr272Lys