Canonical Allele Identifier: CA410686714

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883068G>C (hg19) ; chr22:g.19895545G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895545G>C , CM000684.2:g.19895545G>C	GRCh38
NC_000022.10:g.19883068G>C , CM000684.1:g.19883068G>C	GRCh37
NC_000022.9:g.18263068G>C	NCBI36
NG_011835.1:g.51292C>G , LRG_417:g.51292C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.811C>G MANE Select	ENSP00000383365.1:p.His271Asp
ENST00000334363.14:c.811C>G	ENSP00000334451.9:p.His271Asp
ENST00000400518.5:c.721C>G	ENSP00000383362.1:p.His241Asp
ENST00000400519.6:c.808C>G	ENSP00000383363.1:p.His270Asp
ENST00000400521.6:c.811C>G	ENSP00000383365.1:p.His271Asp
ENST00000400525.6:c.742C>G	ENSP00000383369.3:p.His248Asp
ENST00000474308.5:c.754C>G	ENSP00000485665.1:p.His252Asp
ENST00000475995.3:c.308C>G
ENST00000491939.6:c.715C>G	ENSP00000485543.1:p.His239Asp
ENST00000494454.5:n.885C>G
ENST00000542719.6:c.523C>G	ENSP00000485128.2:p.His175Asp
ENST00000634537.1:c.40C>G	ENSP00000489208.1:p.His14Asp
ENST00000635155.1:n.397C>G
NM_001282512.1:c.811C>G	NP_001269441.1:p.His271Asp
NM_006440.4:c.811C>G	NP_006431.2:p.His271Asp
NM_001282512.2:c.811C>G	NP_001269441.1:p.His271Asp
NM_001352300.1:c.808C>G	NP_001339229.1:p.His270Asp
NM_001352301.1:c.721C>G	NP_001339230.1:p.His241Asp
NM_001352302.1:c.523C>G	NP_001339231.1:p.His175Asp
NM_001352303.1:c.715C>G	NP_001339232.1:p.His239Asp
NR_147957.1:n.943C>G
NM_006440.5:c.811C>G MANE Select	NP_006431.2:p.His271Asp
NM_001282512.3:c.811C>G	NP_001269441.1:p.His271Asp
NM_001352300.2:c.808C>G	NP_001339229.1:p.His270Asp
NR_147957.2:n.769C>G
NM_001352301.2:c.721C>G	NP_001339230.1:p.His241Asp
NM_001352302.2:c.523C>G	NP_001339231.1:p.His175Asp
NM_001352303.2:c.715C>G	NP_001339232.1:p.His239Asp