Canonical Allele Identifier: CA410686507

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882978T>C (hg19) ; chr22:g.19895455T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895455T>C , CM000684.2:g.19895455T>C	GRCh38
NC_000022.10:g.19882978T>C , CM000684.1:g.19882978T>C	GRCh37
NC_000022.9:g.18262978T>C	NCBI36
NG_011835.1:g.51382A>G , LRG_417:g.51382A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.901A>G MANE Select	ENSP00000383365.1:p.Thr301Ala
ENST00000334363.14:c.901A>G	ENSP00000334451.9:p.Thr301Ala
ENST00000400518.5:c.811A>G	ENSP00000383362.1:p.Thr271Ala
ENST00000400519.6:c.898A>G	ENSP00000383363.1:p.Thr300Ala
ENST00000400521.6:c.901A>G	ENSP00000383365.1:p.Thr301Ala
ENST00000400525.6:c.832A>G	ENSP00000383369.3:p.Thr278Ala
ENST00000474308.5:c.844A>G	ENSP00000485665.1:p.Thr282Ala
ENST00000475995.3:c.398A>G
ENST00000491939.6:c.805A>G	ENSP00000485543.1:p.Thr269Ala
ENST00000494454.5:n.975A>G
ENST00000542719.6:c.613A>G	ENSP00000485128.2:p.Thr205Ala
ENST00000634537.1:c.130A>G	ENSP00000489208.1:p.Thr44Ala
ENST00000635155.1:n.487A>G
NM_001282512.1:c.901A>G	NP_001269441.1:p.Thr301Ala
NM_006440.4:c.901A>G	NP_006431.2:p.Thr301Ala
NM_001282512.2:c.901A>G	NP_001269441.1:p.Thr301Ala
NM_001352300.1:c.898A>G	NP_001339229.1:p.Thr300Ala
NM_001352301.1:c.811A>G	NP_001339230.1:p.Thr271Ala
NM_001352302.1:c.613A>G	NP_001339231.1:p.Thr205Ala
NM_001352303.1:c.805A>G	NP_001339232.1:p.Thr269Ala
NR_147957.1:n.1033A>G
NM_006440.5:c.901A>G MANE Select	NP_006431.2:p.Thr301Ala
NM_001282512.3:c.901A>G	NP_001269441.1:p.Thr301Ala
NM_001352300.2:c.898A>G	NP_001339229.1:p.Thr300Ala
NR_147957.2:n.859A>G
NM_001352301.2:c.811A>G	NP_001339230.1:p.Thr271Ala
NM_001352302.2:c.613A>G	NP_001339231.1:p.Thr205Ala
NM_001352303.2:c.805A>G	NP_001339232.1:p.Thr269Ala