Canonical Allele Identifier: CA513369093

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1940765606
• MyVariant Identifiers: chr22:g.19906478G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918955G>C , CM000684.2:g.19918955G>C	GRCh38
NC_000022.10:g.19906478G>C , CM000684.1:g.19906478G>C	GRCh37
NC_000022.9:g.18286478G>C	NCBI36
NG_011835.1:g.27882C>G , LRG_417:g.27882C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.279C>G MANE Select	ENSP00000383365.1:p.Pro93=
ENST00000334363.14:c.279C>G	ENSP00000334451.9:p.Pro93=
ENST00000400518.5:c.189C>G	ENSP00000383362.1:p.Pro63=
ENST00000400519.6:c.276C>G	ENSP00000383363.1:p.Pro92=
ENST00000400521.6:c.279C>G	ENSP00000383365.1:p.Pro93=
ENST00000400525.6:c.210C>G	ENSP00000383369.3:p.Pro70=
ENST00000474308.5:c.222C>G	ENSP00000485665.1:p.Pro74=
ENST00000491939.6:c.183C>G	ENSP00000485543.1:p.Pro61=
ENST00000496729.2:n.284C>G
ENST00000542719.6:c.-10C>G	ENSP00000485128.2:n.-10C>G
NM_001282512.1:c.279C>G	NP_001269441.1:p.Pro93=
NM_006440.4:c.279C>G	NP_006431.2:p.Pro93=
NM_001282512.2:c.279C>G	NP_001269441.1:p.Pro93=
NM_001352300.1:c.276C>G	NP_001339229.1:p.Pro92=
NM_001352301.1:c.189C>G	NP_001339230.1:p.Pro63=
NM_001352302.1:c.-10C>G	NP_001339231.1:n.-10C>G
NM_001352303.1:c.183C>G	NP_001339232.1:p.Pro61=
NR_147957.1:n.411C>G
NM_006440.5:c.279C>G MANE Select	NP_006431.2:p.Pro93=
NM_001282512.3:c.279C>G	NP_001269441.1:p.Pro93=
NM_001352300.2:c.276C>G	NP_001339229.1:p.Pro92=
NR_147957.2:n.237C>G
NM_001352301.2:c.189C>G	NP_001339230.1:p.Pro63=
NM_001352302.2:c.-10C>G	NP_001339231.1:n.-10C>G
NM_001352303.2:c.183C>G	NP_001339232.1:p.Pro61=