Canonical Allele Identifier: CA410694085
Gene: TXNRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19918995C>G , CM000684.2:g.19918995C>G GRCh38
NC_000022.10:g.19906518C>G , CM000684.1:g.19906518C>G GRCh37
NC_000022.9:g.18286518C>G NCBI36
NG_011835.1:g.27842G>C , LRG_417:g.27842G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000400521.7:c.239G>C MANE Select ENSP00000383365.1:p.Trp80Ser
ENST00000334363.14:c.239G>C ENSP00000334451.9:p.Trp80Ser
ENST00000400518.5:c.149G>C ENSP00000383362.1:p.Trp50Ser
ENST00000400519.6:c.236G>C ENSP00000383363.1:p.Trp79Ser
ENST00000400521.6:c.239G>C ENSP00000383365.1:p.Trp80Ser
ENST00000400525.6:c.170G>C ENSP00000383369.3:p.Trp57Ser
ENST00000474308.5:c.182G>C ENSP00000485665.1:p.Trp61Ser
ENST00000491939.6:c.143G>C ENSP00000485543.1:p.Trp48Ser
ENST00000496729.2:n.244G>C
ENST00000542719.6:c.-50G>C ENSP00000485128.2:n.-50G>C
NM_001282512.1:c.239G>C NP_001269441.1:p.Trp80Ser
NM_006440.4:c.239G>C NP_006431.2:p.Trp80Ser
NM_001282512.2:c.239G>C NP_001269441.1:p.Trp80Ser
NM_001352300.1:c.236G>C NP_001339229.1:p.Trp79Ser
NM_001352301.1:c.149G>C NP_001339230.1:p.Trp50Ser
NM_001352302.1:c.-50G>C NP_001339231.1:n.-50G>C
NM_001352303.1:c.143G>C NP_001339232.1:p.Trp48Ser
NR_147957.1:n.371G>C
NM_006440.5:c.239G>C MANE Select NP_006431.2:p.Trp80Ser
NM_001282512.3:c.239G>C NP_001269441.1:p.Trp80Ser
NM_001352300.2:c.236G>C NP_001339229.1:p.Trp79Ser
NR_147957.2:n.197G>C
NM_001352301.2:c.149G>C NP_001339230.1:p.Trp50Ser
NM_001352302.2:c.-50G>C NP_001339231.1:n.-50G>C
NM_001352303.2:c.143G>C NP_001339232.1:p.Trp48Ser