Canonical Allele Identifier: CA410693869

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1457117125
• gnomAD v2: 22-19906456-C-T
• gnomAD v3: 22-19918933-C-T
• gnomAD v4: 22-19918933-C-T
• MyVariant Identifiers: chr22:g.19906456C>T (hg19) ; chr22:g.19918933C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918933C>T , CM000684.2:g.19918933C>T	GRCh38
NC_000022.10:g.19906456C>T , CM000684.1:g.19906456C>T	GRCh37
NC_000022.9:g.18286456C>T	NCBI36
NG_011835.1:g.27904G>A , LRG_417:g.27904G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.301G>A MANE Select	ENSP00000383365.1:p.Ala101Thr
ENST00000334363.14:c.301G>A	ENSP00000334451.9:p.Ala101Thr
ENST00000400518.5:c.211G>A	ENSP00000383362.1:p.Ala71Thr
ENST00000400519.6:c.298G>A	ENSP00000383363.1:p.Ala100Thr
ENST00000400521.6:c.301G>A	ENSP00000383365.1:p.Ala101Thr
ENST00000400525.6:c.232G>A	ENSP00000383369.3:p.Ala78Thr
ENST00000474308.5:c.244G>A	ENSP00000485665.1:p.Ala82Thr
ENST00000491939.6:c.205G>A	ENSP00000485543.1:p.Ala69Thr
ENST00000496729.2:n.306G>A
ENST00000542719.6:c.13G>A	ENSP00000485128.2:p.Ala5Thr
NM_001282512.1:c.301G>A	NP_001269441.1:p.Ala101Thr
NM_006440.4:c.301G>A	NP_006431.2:p.Ala101Thr
NM_001282512.2:c.301G>A	NP_001269441.1:p.Ala101Thr
NM_001352300.1:c.298G>A	NP_001339229.1:p.Ala100Thr
NM_001352301.1:c.211G>A	NP_001339230.1:p.Ala71Thr
NM_001352302.1:c.13G>A	NP_001339231.1:p.Ala5Thr
NM_001352303.1:c.205G>A	NP_001339232.1:p.Ala69Thr
NR_147957.1:n.433G>A
NM_006440.5:c.301G>A MANE Select	NP_006431.2:p.Ala101Thr
NM_001282512.3:c.301G>A	NP_001269441.1:p.Ala101Thr
NM_001352300.2:c.298G>A	NP_001339229.1:p.Ala100Thr
NR_147957.2:n.259G>A
NM_001352301.2:c.211G>A	NP_001339230.1:p.Ala71Thr
NM_001352302.2:c.13G>A	NP_001339231.1:p.Ala5Thr
NM_001352303.2:c.205G>A	NP_001339232.1:p.Ala69Thr