Canonical Allele Identifier: CA410693695

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1390976636
• gnomAD v2: 22-19906408-C-T
• gnomAD v4: 22-19918885-C-T
• MyVariant Identifiers: chr22:g.19906408C>T (hg19) ; chr22:g.19918885C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918885C>T , CM000684.2:g.19918885C>T	GRCh38
NC_000022.10:g.19906408C>T , CM000684.1:g.19906408C>T	GRCh37
NC_000022.9:g.18286408C>T	NCBI36
NG_011835.1:g.27952G>A , LRG_417:g.27952G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.349G>A MANE Select	ENSP00000383365.1:p.Val117Met
ENST00000334363.14:c.349G>A	ENSP00000334451.9:p.Val117Met
ENST00000400518.5:c.259G>A	ENSP00000383362.1:p.Val87Met
ENST00000400519.6:c.346G>A	ENSP00000383363.1:p.Val116Met
ENST00000400521.6:c.349G>A	ENSP00000383365.1:p.Val117Met
ENST00000400525.6:c.280G>A	ENSP00000383369.3:p.Val94Met
ENST00000474308.5:c.292G>A	ENSP00000485665.1:p.Val98Met
ENST00000491939.6:c.253G>A	ENSP00000485543.1:p.Val85Met
ENST00000496729.2:n.354G>A
ENST00000542719.6:c.61G>A	ENSP00000485128.2:p.Val21Met
NM_001282512.1:c.349G>A	NP_001269441.1:p.Val117Met
NM_006440.4:c.349G>A	NP_006431.2:p.Val117Met
NM_001282512.2:c.349G>A	NP_001269441.1:p.Val117Met
NM_001352300.1:c.346G>A	NP_001339229.1:p.Val116Met
NM_001352301.1:c.259G>A	NP_001339230.1:p.Val87Met
NM_001352302.1:c.61G>A	NP_001339231.1:p.Val21Met
NM_001352303.1:c.253G>A	NP_001339232.1:p.Val85Met
NR_147957.1:n.481G>A
NM_006440.5:c.349G>A MANE Select	NP_006431.2:p.Val117Met
NM_001282512.3:c.349G>A	NP_001269441.1:p.Val117Met
NM_001352300.2:c.346G>A	NP_001339229.1:p.Val116Met
NR_147957.2:n.307G>A
NM_001352301.2:c.259G>A	NP_001339230.1:p.Val87Met
NM_001352302.2:c.61G>A	NP_001339231.1:p.Val21Met
NM_001352303.2:c.253G>A	NP_001339232.1:p.Val85Met