Canonical Allele Identifier: CA513365373

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883048C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895525C>T , CM000684.2:g.19895525C>T	GRCh38
NC_000022.10:g.19883048C>T , CM000684.1:g.19883048C>T	GRCh37
NC_000022.9:g.18263048C>T	NCBI36
NG_011835.1:g.51312G>A , LRG_417:g.51312G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.831G>A MANE Select	ENSP00000383365.1:p.Arg277=
ENST00000334363.14:c.831G>A	ENSP00000334451.9:p.Arg277=
ENST00000400518.5:c.741G>A	ENSP00000383362.1:p.Arg247=
ENST00000400519.6:c.828G>A	ENSP00000383363.1:p.Arg276=
ENST00000400521.6:c.831G>A	ENSP00000383365.1:p.Arg277=
ENST00000400525.6:c.762G>A	ENSP00000383369.3:p.Arg254=
ENST00000474308.5:c.774G>A	ENSP00000485665.1:p.Arg258=
ENST00000475995.3:c.328G>A
ENST00000491939.6:c.735G>A	ENSP00000485543.1:p.Arg245=
ENST00000494454.5:n.905G>A
ENST00000542719.6:c.543G>A	ENSP00000485128.2:p.Arg181=
ENST00000634537.1:c.60G>A	ENSP00000489208.1:p.Arg20=
ENST00000635155.1:n.417G>A
NM_001282512.1:c.831G>A	NP_001269441.1:p.Arg277=
NM_006440.4:c.831G>A	NP_006431.2:p.Arg277=
NM_001282512.2:c.831G>A	NP_001269441.1:p.Arg277=
NM_001352300.1:c.828G>A	NP_001339229.1:p.Arg276=
NM_001352301.1:c.741G>A	NP_001339230.1:p.Arg247=
NM_001352302.1:c.543G>A	NP_001339231.1:p.Arg181=
NM_001352303.1:c.735G>A	NP_001339232.1:p.Arg245=
NR_147957.1:n.963G>A
NM_006440.5:c.831G>A MANE Select	NP_006431.2:p.Arg277=
NM_001282512.3:c.831G>A	NP_001269441.1:p.Arg277=
NM_001352300.2:c.828G>A	NP_001339229.1:p.Arg276=
NR_147957.2:n.789G>A
NM_001352301.2:c.741G>A	NP_001339230.1:p.Arg247=
NM_001352302.2:c.543G>A	NP_001339231.1:p.Arg181=
NM_001352303.2:c.735G>A	NP_001339232.1:p.Arg245=