Canonical Allele Identifier: CA410693769
Gene: TXNRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19918905G>C , CM000684.2:g.19918905G>C GRCh38
NC_000022.10:g.19906428G>C , CM000684.1:g.19906428G>C GRCh37
NC_000022.9:g.18286428G>C NCBI36
NG_011835.1:g.27932C>G , LRG_417:g.27932C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000400521.7:c.329C>G MANE Select ENSP00000383365.1:p.Ala110Gly
ENST00000334363.14:c.329C>G ENSP00000334451.9:p.Ala110Gly
ENST00000400518.5:c.239C>G ENSP00000383362.1:p.Ala80Gly
ENST00000400519.6:c.326C>G ENSP00000383363.1:p.Ala109Gly
ENST00000400521.6:c.329C>G ENSP00000383365.1:p.Ala110Gly
ENST00000400525.6:c.260C>G ENSP00000383369.3:p.Ala87Gly
ENST00000474308.5:c.272C>G ENSP00000485665.1:p.Ala91Gly
ENST00000491939.6:c.233C>G ENSP00000485543.1:p.Ala78Gly
ENST00000496729.2:n.334C>G
ENST00000542719.6:c.41C>G ENSP00000485128.2:p.Ala14Gly
NM_001282512.1:c.329C>G NP_001269441.1:p.Ala110Gly
NM_006440.4:c.329C>G NP_006431.2:p.Ala110Gly
NM_001282512.2:c.329C>G NP_001269441.1:p.Ala110Gly
NM_001352300.1:c.326C>G NP_001339229.1:p.Ala109Gly
NM_001352301.1:c.239C>G NP_001339230.1:p.Ala80Gly
NM_001352302.1:c.41C>G NP_001339231.1:p.Ala14Gly
NM_001352303.1:c.233C>G NP_001339232.1:p.Ala78Gly
NR_147957.1:n.461C>G
NM_006440.5:c.329C>G MANE Select NP_006431.2:p.Ala110Gly
NM_001282512.3:c.329C>G NP_001269441.1:p.Ala110Gly
NM_001352300.2:c.326C>G NP_001339229.1:p.Ala109Gly
NR_147957.2:n.287C>G
NM_001352301.2:c.239C>G NP_001339230.1:p.Ala80Gly
NM_001352302.2:c.41C>G NP_001339231.1:p.Ala14Gly
NM_001352303.2:c.233C>G NP_001339232.1:p.Ala78Gly