Canonical Allele Identifier: CA410686738

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883078G>C (hg19) ; chr22:g.19895555G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895555G>C , CM000684.2:g.19895555G>C	GRCh38
NC_000022.10:g.19883078G>C , CM000684.1:g.19883078G>C	GRCh37
NC_000022.9:g.18263078G>C	NCBI36
NG_011835.1:g.51282C>G , LRG_417:g.51282C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.801C>G MANE Select	ENSP00000383365.1:p.His267Gln
ENST00000334363.14:c.801C>G	ENSP00000334451.9:p.His267Gln
ENST00000400518.5:c.711C>G	ENSP00000383362.1:p.His237Gln
ENST00000400519.6:c.798C>G	ENSP00000383363.1:p.His266Gln
ENST00000400521.6:c.801C>G	ENSP00000383365.1:p.His267Gln
ENST00000400525.6:c.732C>G	ENSP00000383369.3:p.His244Gln
ENST00000474308.5:c.744C>G	ENSP00000485665.1:p.His248Gln
ENST00000475995.3:c.298C>G
ENST00000491939.6:c.705C>G	ENSP00000485543.1:p.His235Gln
ENST00000494454.5:n.875C>G
ENST00000542719.6:c.513C>G	ENSP00000485128.2:p.His171Gln
ENST00000634537.1:c.30C>G	ENSP00000489208.1:p.His10Gln
ENST00000635155.1:n.387C>G
NM_001282512.1:c.801C>G	NP_001269441.1:p.His267Gln
NM_006440.4:c.801C>G	NP_006431.2:p.His267Gln
NM_001282512.2:c.801C>G	NP_001269441.1:p.His267Gln
NM_001352300.1:c.798C>G	NP_001339229.1:p.His266Gln
NM_001352301.1:c.711C>G	NP_001339230.1:p.His237Gln
NM_001352302.1:c.513C>G	NP_001339231.1:p.His171Gln
NM_001352303.1:c.705C>G	NP_001339232.1:p.His235Gln
NR_147957.1:n.933C>G
NM_006440.5:c.801C>G MANE Select	NP_006431.2:p.His267Gln
NM_001282512.3:c.801C>G	NP_001269441.1:p.His267Gln
NM_001352300.2:c.798C>G	NP_001339229.1:p.His266Gln
NR_147957.2:n.759C>G
NM_001352301.2:c.711C>G	NP_001339230.1:p.His237Gln
NM_001352302.2:c.513C>G	NP_001339231.1:p.His171Gln
NM_001352303.2:c.705C>G	NP_001339232.1:p.His235Gln