Canonical Allele Identifier: CA410694038

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19918981-T-C
• COSMIC: COSM4642590 ; COSM4642591
• MyVariant Identifiers: chr22:g.19906504T>C (hg19) ; chr22:g.19918981T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918981T>C , CM000684.2:g.19918981T>C	GRCh38
NC_000022.10:g.19906504T>C , CM000684.1:g.19906504T>C	GRCh37
NC_000022.9:g.18286504T>C	NCBI36
NG_011835.1:g.27856A>G , LRG_417:g.27856A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.253A>G MANE Select	ENSP00000383365.1:p.Thr85Ala
ENST00000334363.14:c.253A>G	ENSP00000334451.9:p.Thr85Ala
ENST00000400518.5:c.163A>G	ENSP00000383362.1:p.Thr55Ala
ENST00000400519.6:c.250A>G	ENSP00000383363.1:p.Thr84Ala
ENST00000400521.6:c.253A>G	ENSP00000383365.1:p.Thr85Ala
ENST00000400525.6:c.184A>G	ENSP00000383369.3:p.Thr62Ala
ENST00000474308.5:c.196A>G	ENSP00000485665.1:p.Thr66Ala
ENST00000491939.6:c.157A>G	ENSP00000485543.1:p.Thr53Ala
ENST00000496729.2:n.258A>G
ENST00000542719.6:c.-36A>G	ENSP00000485128.2:n.-36A>G
NM_001282512.1:c.253A>G	NP_001269441.1:p.Thr85Ala
NM_006440.4:c.253A>G	NP_006431.2:p.Thr85Ala
NM_001282512.2:c.253A>G	NP_001269441.1:p.Thr85Ala
NM_001352300.1:c.250A>G	NP_001339229.1:p.Thr84Ala
NM_001352301.1:c.163A>G	NP_001339230.1:p.Thr55Ala
NM_001352302.1:c.-36A>G	NP_001339231.1:n.-36A>G
NM_001352303.1:c.157A>G	NP_001339232.1:p.Thr53Ala
NR_147957.1:n.385A>G
NM_006440.5:c.253A>G MANE Select	NP_006431.2:p.Thr85Ala
NM_001282512.3:c.253A>G	NP_001269441.1:p.Thr85Ala
NM_001352300.2:c.250A>G	NP_001339229.1:p.Thr84Ala
NR_147957.2:n.211A>G
NM_001352301.2:c.163A>G	NP_001339230.1:p.Thr55Ala
NM_001352302.2:c.-36A>G	NP_001339231.1:n.-36A>G
NM_001352303.2:c.157A>G	NP_001339232.1:p.Thr53Ala