Canonical Allele Identifier: CA410686343

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882948T>C (hg19) ; chr22:g.19895425T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895425T>C , CM000684.2:g.19895425T>C	GRCh38
NC_000022.10:g.19882948T>C , CM000684.1:g.19882948T>C	GRCh37
NC_000022.9:g.18262948T>C	NCBI36
NG_011835.1:g.51412A>G , LRG_417:g.51412A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.931A>G MANE Select	ENSP00000383365.1:p.Thr311Ala
ENST00000334363.14:c.931A>G	ENSP00000334451.9:p.Thr311Ala
ENST00000400518.5:c.841A>G	ENSP00000383362.1:p.Thr281Ala
ENST00000400519.6:c.928A>G	ENSP00000383363.1:p.Thr310Ala
ENST00000400521.6:c.931A>G	ENSP00000383365.1:p.Thr311Ala
ENST00000400525.6:c.862A>G	ENSP00000383369.3:p.Thr288Ala
ENST00000474308.5:c.874A>G	ENSP00000485665.1:p.Thr292Ala
ENST00000475995.3:c.428A>G
ENST00000491939.6:c.835A>G	ENSP00000485543.1:p.Thr279Ala
ENST00000494454.5:n.1005A>G
ENST00000542719.6:c.643A>G	ENSP00000485128.2:p.Thr215Ala
ENST00000634537.1:c.160A>G	ENSP00000489208.1:p.Thr54Ala
ENST00000635155.1:n.517A>G
NM_001282512.1:c.931A>G	NP_001269441.1:p.Thr311Ala
NM_006440.4:c.931A>G	NP_006431.2:p.Thr311Ala
NM_001282512.2:c.931A>G	NP_001269441.1:p.Thr311Ala
NM_001352300.1:c.928A>G	NP_001339229.1:p.Thr310Ala
NM_001352301.1:c.841A>G	NP_001339230.1:p.Thr281Ala
NM_001352302.1:c.643A>G	NP_001339231.1:p.Thr215Ala
NM_001352303.1:c.835A>G	NP_001339232.1:p.Thr279Ala
NR_147957.1:n.1063A>G
NM_006440.5:c.931A>G MANE Select	NP_006431.2:p.Thr311Ala
NM_001282512.3:c.931A>G	NP_001269441.1:p.Thr311Ala
NM_001352300.2:c.928A>G	NP_001339229.1:p.Thr310Ala
NR_147957.2:n.889A>G
NM_001352301.2:c.841A>G	NP_001339230.1:p.Thr281Ala
NM_001352302.2:c.643A>G	NP_001339231.1:p.Thr215Ala
NM_001352303.2:c.835A>G	NP_001339232.1:p.Thr279Ala