Canonical Allele Identifier: CA410686678

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883049C>A (hg19) ; chr22:g.19895526C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895526C>A , CM000684.2:g.19895526C>A	GRCh38
NC_000022.10:g.19883049C>A , CM000684.1:g.19883049C>A	GRCh37
NC_000022.9:g.18263049C>A	NCBI36
NG_011835.1:g.51311G>T , LRG_417:g.51311G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.830G>T MANE Select	ENSP00000383365.1:p.Arg277Met
ENST00000334363.14:c.830G>T	ENSP00000334451.9:p.Arg277Met
ENST00000400518.5:c.740G>T	ENSP00000383362.1:p.Arg247Met
ENST00000400519.6:c.827G>T	ENSP00000383363.1:p.Arg276Met
ENST00000400521.6:c.830G>T	ENSP00000383365.1:p.Arg277Met
ENST00000400525.6:c.761G>T	ENSP00000383369.3:p.Arg254Met
ENST00000474308.5:c.773G>T	ENSP00000485665.1:p.Arg258Met
ENST00000475995.3:c.327G>T
ENST00000491939.6:c.734G>T	ENSP00000485543.1:p.Arg245Met
ENST00000494454.5:n.904G>T
ENST00000542719.6:c.542G>T	ENSP00000485128.2:p.Arg181Met
ENST00000634537.1:c.59G>T	ENSP00000489208.1:p.Arg20Met
ENST00000635155.1:n.416G>T
NM_001282512.1:c.830G>T	NP_001269441.1:p.Arg277Met
NM_006440.4:c.830G>T	NP_006431.2:p.Arg277Met
NM_001282512.2:c.830G>T	NP_001269441.1:p.Arg277Met
NM_001352300.1:c.827G>T	NP_001339229.1:p.Arg276Met
NM_001352301.1:c.740G>T	NP_001339230.1:p.Arg247Met
NM_001352302.1:c.542G>T	NP_001339231.1:p.Arg181Met
NM_001352303.1:c.734G>T	NP_001339232.1:p.Arg245Met
NR_147957.1:n.962G>T
NM_006440.5:c.830G>T MANE Select	NP_006431.2:p.Arg277Met
NM_001282512.3:c.830G>T	NP_001269441.1:p.Arg277Met
NM_001352300.2:c.827G>T	NP_001339229.1:p.Arg276Met
NR_147957.2:n.788G>T
NM_001352301.2:c.740G>T	NP_001339230.1:p.Arg247Met
NM_001352302.2:c.542G>T	NP_001339231.1:p.Arg181Met
NM_001352303.2:c.734G>T	NP_001339232.1:p.Arg245Met