Canonical Allele Identifier: CA410686318

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882942G>C (hg19) ; chr22:g.19895419G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895419G>C , CM000684.2:g.19895419G>C	GRCh38
NC_000022.10:g.19882942G>C , CM000684.1:g.19882942G>C	GRCh37
NC_000022.9:g.18262942G>C	NCBI36
NG_011835.1:g.51418C>G , LRG_417:g.51418C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.937C>G MANE Select	ENSP00000383365.1:p.Leu313Val
ENST00000334363.14:c.937C>G	ENSP00000334451.9:p.Leu313Val
ENST00000400518.5:c.847C>G	ENSP00000383362.1:p.Leu283Val
ENST00000400519.6:c.934C>G	ENSP00000383363.1:p.Leu312Val
ENST00000400521.6:c.937C>G	ENSP00000383365.1:p.Leu313Val
ENST00000400525.6:c.868C>G	ENSP00000383369.3:p.Leu290Val
ENST00000474308.5:c.880C>G	ENSP00000485665.1:p.Leu294Val
ENST00000475995.3:c.434C>G
ENST00000491939.6:c.841C>G	ENSP00000485543.1:p.Leu281Val
ENST00000494454.5:n.1011C>G
ENST00000542719.6:c.649C>G	ENSP00000485128.2:p.Leu217Val
ENST00000634537.1:c.166C>G	ENSP00000489208.1:p.Leu56Val
ENST00000635155.1:n.523C>G
NM_001282512.1:c.937C>G	NP_001269441.1:p.Leu313Val
NM_006440.4:c.937C>G	NP_006431.2:p.Leu313Val
NM_001282512.2:c.937C>G	NP_001269441.1:p.Leu313Val
NM_001352300.1:c.934C>G	NP_001339229.1:p.Leu312Val
NM_001352301.1:c.847C>G	NP_001339230.1:p.Leu283Val
NM_001352302.1:c.649C>G	NP_001339231.1:p.Leu217Val
NM_001352303.1:c.841C>G	NP_001339232.1:p.Leu281Val
NR_147957.1:n.1069C>G
NM_006440.5:c.937C>G MANE Select	NP_006431.2:p.Leu313Val
NM_001282512.3:c.937C>G	NP_001269441.1:p.Leu313Val
NM_001352300.2:c.934C>G	NP_001339229.1:p.Leu312Val
NR_147957.2:n.895C>G
NM_001352301.2:c.847C>G	NP_001339230.1:p.Leu283Val
NM_001352302.2:c.649C>G	NP_001339231.1:p.Leu217Val
NM_001352303.2:c.841C>G	NP_001339232.1:p.Leu281Val