Canonical Allele Identifier: CA410694099

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19919001-G-T
• MyVariant Identifiers: chr22:g.19906524G>T (hg19) ; chr22:g.19919001G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19919001G>T , CM000684.2:g.19919001G>T	GRCh38
NC_000022.10:g.19906524G>T , CM000684.1:g.19906524G>T	GRCh37
NC_000022.9:g.18286524G>T	NCBI36
NG_011835.1:g.27836C>A , LRG_417:g.27836C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.233C>A MANE Select	ENSP00000383365.1:p.Thr78Asn
ENST00000334363.14:c.233C>A	ENSP00000334451.9:p.Thr78Asn
ENST00000400518.5:c.143C>A	ENSP00000383362.1:p.Thr48Asn
ENST00000400519.6:c.230C>A	ENSP00000383363.1:p.Thr77Asn
ENST00000400521.6:c.233C>A	ENSP00000383365.1:p.Thr78Asn
ENST00000400525.6:c.164C>A	ENSP00000383369.3:p.Thr55Asn
ENST00000474308.5:c.176C>A	ENSP00000485665.1:p.Thr59Asn
ENST00000491939.6:c.137C>A	ENSP00000485543.1:p.Thr46Asn
ENST00000496729.2:n.238C>A
ENST00000542719.6:c.-56C>A	ENSP00000485128.2:n.-56C>A
NM_001282512.1:c.233C>A	NP_001269441.1:p.Thr78Asn
NM_006440.4:c.233C>A	NP_006431.2:p.Thr78Asn
NM_001282512.2:c.233C>A	NP_001269441.1:p.Thr78Asn
NM_001352300.1:c.230C>A	NP_001339229.1:p.Thr77Asn
NM_001352301.1:c.143C>A	NP_001339230.1:p.Thr48Asn
NM_001352302.1:c.-56C>A	NP_001339231.1:n.-56C>A
NM_001352303.1:c.137C>A	NP_001339232.1:p.Thr46Asn
NR_147957.1:n.365C>A
NM_006440.5:c.233C>A MANE Select	NP_006431.2:p.Thr78Asn
NM_001282512.3:c.233C>A	NP_001269441.1:p.Thr78Asn
NM_001352300.2:c.230C>A	NP_001339229.1:p.Thr77Asn
NR_147957.2:n.191C>A
NM_001352301.2:c.143C>A	NP_001339230.1:p.Thr48Asn
NM_001352302.2:c.-56C>A	NP_001339231.1:n.-56C>A
NM_001352303.2:c.137C>A	NP_001339232.1:p.Thr46Asn