Canonical Allele Identifier: CA410686679

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883050T>C (hg19) ; chr22:g.19895527T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895527T>C , CM000684.2:g.19895527T>C	GRCh38
NC_000022.10:g.19883050T>C , CM000684.1:g.19883050T>C	GRCh37
NC_000022.9:g.18263050T>C	NCBI36
NG_011835.1:g.51310A>G , LRG_417:g.51310A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.829A>G MANE Select	ENSP00000383365.1:p.Arg277Gly
ENST00000334363.14:c.829A>G	ENSP00000334451.9:p.Arg277Gly
ENST00000400518.5:c.739A>G	ENSP00000383362.1:p.Arg247Gly
ENST00000400519.6:c.826A>G	ENSP00000383363.1:p.Arg276Gly
ENST00000400521.6:c.829A>G	ENSP00000383365.1:p.Arg277Gly
ENST00000400525.6:c.760A>G	ENSP00000383369.3:p.Arg254Gly
ENST00000474308.5:c.772A>G	ENSP00000485665.1:p.Arg258Gly
ENST00000475995.3:c.326A>G
ENST00000491939.6:c.733A>G	ENSP00000485543.1:p.Arg245Gly
ENST00000494454.5:n.903A>G
ENST00000542719.6:c.541A>G	ENSP00000485128.2:p.Arg181Gly
ENST00000634537.1:c.58A>G	ENSP00000489208.1:p.Arg20Gly
ENST00000635155.1:n.415A>G
NM_001282512.1:c.829A>G	NP_001269441.1:p.Arg277Gly
NM_006440.4:c.829A>G	NP_006431.2:p.Arg277Gly
NM_001282512.2:c.829A>G	NP_001269441.1:p.Arg277Gly
NM_001352300.1:c.826A>G	NP_001339229.1:p.Arg276Gly
NM_001352301.1:c.739A>G	NP_001339230.1:p.Arg247Gly
NM_001352302.1:c.541A>G	NP_001339231.1:p.Arg181Gly
NM_001352303.1:c.733A>G	NP_001339232.1:p.Arg245Gly
NR_147957.1:n.961A>G
NM_006440.5:c.829A>G MANE Select	NP_006431.2:p.Arg277Gly
NM_001282512.3:c.829A>G	NP_001269441.1:p.Arg277Gly
NM_001352300.2:c.826A>G	NP_001339229.1:p.Arg276Gly
NR_147957.2:n.787A>G
NM_001352301.2:c.739A>G	NP_001339230.1:p.Arg247Gly
NM_001352302.2:c.541A>G	NP_001339231.1:p.Arg181Gly
NM_001352303.2:c.733A>G	NP_001339232.1:p.Arg245Gly