Canonical Allele Identifier: CA513369119

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19919000-G-T
• COSMIC: COSM3842198 ; COSM3842199
• MyVariant Identifiers: chr22:g.19906523G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19919000G>T , CM000684.2:g.19919000G>T	GRCh38
NC_000022.10:g.19906523G>T , CM000684.1:g.19906523G>T	GRCh37
NC_000022.9:g.18286523G>T	NCBI36
NG_011835.1:g.27837C>A , LRG_417:g.27837C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.234C>A MANE Select	ENSP00000383365.1:p.Thr78=
ENST00000334363.14:c.234C>A	ENSP00000334451.9:p.Thr78=
ENST00000400518.5:c.144C>A	ENSP00000383362.1:p.Thr48=
ENST00000400519.6:c.231C>A	ENSP00000383363.1:p.Thr77=
ENST00000400521.6:c.234C>A	ENSP00000383365.1:p.Thr78=
ENST00000400525.6:c.165C>A	ENSP00000383369.3:p.Thr55=
ENST00000474308.5:c.177C>A	ENSP00000485665.1:p.Thr59=
ENST00000491939.6:c.138C>A	ENSP00000485543.1:p.Thr46=
ENST00000496729.2:n.239C>A
ENST00000542719.6:c.-55C>A	ENSP00000485128.2:n.-55C>A
NM_001282512.1:c.234C>A	NP_001269441.1:p.Thr78=
NM_006440.4:c.234C>A	NP_006431.2:p.Thr78=
NM_001282512.2:c.234C>A	NP_001269441.1:p.Thr78=
NM_001352300.1:c.231C>A	NP_001339229.1:p.Thr77=
NM_001352301.1:c.144C>A	NP_001339230.1:p.Thr48=
NM_001352302.1:c.-55C>A	NP_001339231.1:n.-55C>A
NM_001352303.1:c.138C>A	NP_001339232.1:p.Thr46=
NR_147957.1:n.366C>A
NM_006440.5:c.234C>A MANE Select	NP_006431.2:p.Thr78=
NM_001282512.3:c.234C>A	NP_001269441.1:p.Thr78=
NM_001352300.2:c.231C>A	NP_001339229.1:p.Thr77=
NR_147957.2:n.192C>A
NM_001352301.2:c.144C>A	NP_001339230.1:p.Thr48=
NM_001352302.2:c.-55C>A	NP_001339231.1:n.-55C>A
NM_001352303.2:c.138C>A	NP_001339232.1:p.Thr46=