Canonical Allele Identifier: CA410686454

Gene: TXNRD2

Linked Data

• dbSNP Id: rs2145969853
• MyVariant Identifiers: chr22:g.19882968T>A (hg19) ; chr22:g.19895445T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895445T>A , CM000684.2:g.19895445T>A	GRCh38
NC_000022.10:g.19882968T>A , CM000684.1:g.19882968T>A	GRCh37
NC_000022.9:g.18262968T>A	NCBI36
NG_011835.1:g.51392A>T , LRG_417:g.51392A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.911A>T MANE Select	ENSP00000383365.1:p.Glu304Val
ENST00000334363.14:c.911A>T	ENSP00000334451.9:p.Glu304Val
ENST00000400518.5:c.821A>T	ENSP00000383362.1:p.Glu274Val
ENST00000400519.6:c.908A>T	ENSP00000383363.1:p.Glu303Val
ENST00000400521.6:c.911A>T	ENSP00000383365.1:p.Glu304Val
ENST00000400525.6:c.842A>T	ENSP00000383369.3:p.Glu281Val
ENST00000474308.5:c.854A>T	ENSP00000485665.1:p.Glu285Val
ENST00000475995.3:c.408A>T
ENST00000491939.6:c.815A>T	ENSP00000485543.1:p.Glu272Val
ENST00000494454.5:n.985A>T
ENST00000542719.6:c.623A>T	ENSP00000485128.2:p.Glu208Val
ENST00000634537.1:c.140A>T	ENSP00000489208.1:p.Glu47Val
ENST00000635155.1:n.497A>T
NM_001282512.1:c.911A>T	NP_001269441.1:p.Glu304Val
NM_006440.4:c.911A>T	NP_006431.2:p.Glu304Val
NM_001282512.2:c.911A>T	NP_001269441.1:p.Glu304Val
NM_001352300.1:c.908A>T	NP_001339229.1:p.Glu303Val
NM_001352301.1:c.821A>T	NP_001339230.1:p.Glu274Val
NM_001352302.1:c.623A>T	NP_001339231.1:p.Glu208Val
NM_001352303.1:c.815A>T	NP_001339232.1:p.Glu272Val
NR_147957.1:n.1043A>T
NM_006440.5:c.911A>T MANE Select	NP_006431.2:p.Glu304Val
NM_001282512.3:c.911A>T	NP_001269441.1:p.Glu304Val
NM_001352300.2:c.908A>T	NP_001339229.1:p.Glu303Val
NR_147957.2:n.869A>T
NM_001352301.2:c.821A>T	NP_001339230.1:p.Glu274Val
NM_001352302.2:c.623A>T	NP_001339231.1:p.Glu208Val
NM_001352303.2:c.815A>T	NP_001339232.1:p.Glu272Val