Canonical Allele Identifier: CA410686688

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883055A>C (hg19) ; chr22:g.19895532A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895532A>C , CM000684.2:g.19895532A>C	GRCh38
NC_000022.10:g.19883055A>C , CM000684.1:g.19883055A>C	GRCh37
NC_000022.9:g.18263055A>C	NCBI36
NG_011835.1:g.51305T>G , LRG_417:g.51305T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.824T>G MANE Select	ENSP00000383365.1:p.Phe275Cys
ENST00000334363.14:c.824T>G	ENSP00000334451.9:p.Phe275Cys
ENST00000400518.5:c.734T>G	ENSP00000383362.1:p.Phe245Cys
ENST00000400519.6:c.821T>G	ENSP00000383363.1:p.Phe274Cys
ENST00000400521.6:c.824T>G	ENSP00000383365.1:p.Phe275Cys
ENST00000400525.6:c.755T>G	ENSP00000383369.3:p.Phe252Cys
ENST00000474308.5:c.767T>G	ENSP00000485665.1:p.Phe256Cys
ENST00000475995.3:c.321T>G
ENST00000491939.6:c.728T>G	ENSP00000485543.1:p.Phe243Cys
ENST00000494454.5:n.898T>G
ENST00000542719.6:c.536T>G	ENSP00000485128.2:p.Phe179Cys
ENST00000634537.1:c.53T>G	ENSP00000489208.1:p.Phe18Cys
ENST00000635155.1:n.410T>G
NM_001282512.1:c.824T>G	NP_001269441.1:p.Phe275Cys
NM_006440.4:c.824T>G	NP_006431.2:p.Phe275Cys
NM_001282512.2:c.824T>G	NP_001269441.1:p.Phe275Cys
NM_001352300.1:c.821T>G	NP_001339229.1:p.Phe274Cys
NM_001352301.1:c.734T>G	NP_001339230.1:p.Phe245Cys
NM_001352302.1:c.536T>G	NP_001339231.1:p.Phe179Cys
NM_001352303.1:c.728T>G	NP_001339232.1:p.Phe243Cys
NR_147957.1:n.956T>G
NM_006440.5:c.824T>G MANE Select	NP_006431.2:p.Phe275Cys
NM_001282512.3:c.824T>G	NP_001269441.1:p.Phe275Cys
NM_001352300.2:c.821T>G	NP_001339229.1:p.Phe274Cys
NR_147957.2:n.782T>G
NM_001352301.2:c.734T>G	NP_001339230.1:p.Phe245Cys
NM_001352302.2:c.536T>G	NP_001339231.1:p.Phe179Cys
NM_001352303.2:c.728T>G	NP_001339232.1:p.Phe243Cys