Canonical Allele Identifier: CA513365247

Gene: TXNRD2

Linked Data

• ClinVar Variation Id: 1763858
• ClinVar RCV Id: RCV002447857
• gnomAD v4: 22-19895501-C-T
• MyVariant Identifiers: chr22:g.19883024C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895501C>T , CM000684.2:g.19895501C>T	GRCh38
NC_000022.10:g.19883024C>T , CM000684.1:g.19883024C>T	GRCh37
NC_000022.9:g.18263024C>T	NCBI36
NG_011835.1:g.51336G>A , LRG_417:g.51336G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.855G>A MANE Select	ENSP00000383365.1:p.Arg285=
ENST00000334363.14:c.855G>A	ENSP00000334451.9:p.Arg285=
ENST00000400518.5:c.765G>A	ENSP00000383362.1:p.Arg255=
ENST00000400519.6:c.852G>A	ENSP00000383363.1:p.Arg284=
ENST00000400521.6:c.855G>A	ENSP00000383365.1:p.Arg285=
ENST00000400525.6:c.786G>A	ENSP00000383369.3:p.Arg262=
ENST00000474308.5:c.798G>A	ENSP00000485665.1:p.Arg266=
ENST00000475995.3:c.352G>A
ENST00000491939.6:c.759G>A	ENSP00000485543.1:p.Arg253=
ENST00000494454.5:n.929G>A
ENST00000542719.6:c.567G>A	ENSP00000485128.2:p.Arg189=
ENST00000634537.1:c.84G>A	ENSP00000489208.1:p.Arg28=
ENST00000635155.1:n.441G>A
NM_001282512.1:c.855G>A	NP_001269441.1:p.Arg285=
NM_006440.4:c.855G>A	NP_006431.2:p.Arg285=
NM_001282512.2:c.855G>A	NP_001269441.1:p.Arg285=
NM_001352300.1:c.852G>A	NP_001339229.1:p.Arg284=
NM_001352301.1:c.765G>A	NP_001339230.1:p.Arg255=
NM_001352302.1:c.567G>A	NP_001339231.1:p.Arg189=
NM_001352303.1:c.759G>A	NP_001339232.1:p.Arg253=
NR_147957.1:n.987G>A
NM_006440.5:c.855G>A MANE Select	NP_006431.2:p.Arg285=
NM_001282512.3:c.855G>A	NP_001269441.1:p.Arg285=
NM_001352300.2:c.852G>A	NP_001339229.1:p.Arg284=
NR_147957.2:n.813G>A
NM_001352301.2:c.765G>A	NP_001339230.1:p.Arg255=
NM_001352302.2:c.567G>A	NP_001339231.1:p.Arg189=
NM_001352303.2:c.759G>A	NP_001339232.1:p.Arg253=