Canonical Allele Identifier: CA410686401

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1601409811
• MyVariant Identifiers: chr22:g.19882957T>G (hg19) ; chr22:g.19895434T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895434T>G , CM000684.2:g.19895434T>G	GRCh38
NC_000022.10:g.19882957T>G , CM000684.1:g.19882957T>G	GRCh37
NC_000022.9:g.18262957T>G	NCBI36
NG_011835.1:g.51403A>C , LRG_417:g.51403A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.922A>C MANE Select	ENSP00000383365.1:p.Thr308Pro
ENST00000334363.14:c.922A>C	ENSP00000334451.9:p.Thr308Pro
ENST00000400518.5:c.832A>C	ENSP00000383362.1:p.Thr278Pro
ENST00000400519.6:c.919A>C	ENSP00000383363.1:p.Thr307Pro
ENST00000400521.6:c.922A>C	ENSP00000383365.1:p.Thr308Pro
ENST00000400525.6:c.853A>C	ENSP00000383369.3:p.Thr285Pro
ENST00000474308.5:c.865A>C	ENSP00000485665.1:p.Thr289Pro
ENST00000475995.3:c.419A>C
ENST00000491939.6:c.826A>C	ENSP00000485543.1:p.Thr276Pro
ENST00000494454.5:n.996A>C
ENST00000542719.6:c.634A>C	ENSP00000485128.2:p.Thr212Pro
ENST00000634537.1:c.151A>C	ENSP00000489208.1:p.Thr51Pro
ENST00000635155.1:n.508A>C
NM_001282512.1:c.922A>C	NP_001269441.1:p.Thr308Pro
NM_006440.4:c.922A>C	NP_006431.2:p.Thr308Pro
NM_001282512.2:c.922A>C	NP_001269441.1:p.Thr308Pro
NM_001352300.1:c.919A>C	NP_001339229.1:p.Thr307Pro
NM_001352301.1:c.832A>C	NP_001339230.1:p.Thr278Pro
NM_001352302.1:c.634A>C	NP_001339231.1:p.Thr212Pro
NM_001352303.1:c.826A>C	NP_001339232.1:p.Thr276Pro
NR_147957.1:n.1054A>C
NM_006440.5:c.922A>C MANE Select	NP_006431.2:p.Thr308Pro
NM_001282512.3:c.922A>C	NP_001269441.1:p.Thr308Pro
NM_001352300.2:c.919A>C	NP_001339229.1:p.Thr307Pro
NR_147957.2:n.880A>C
NM_001352301.2:c.832A>C	NP_001339230.1:p.Thr278Pro
NM_001352302.2:c.634A>C	NP_001339231.1:p.Thr212Pro
NM_001352303.2:c.826A>C	NP_001339232.1:p.Thr276Pro