Canonical Allele Identifier: CA513365181

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882997G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895474G>C , CM000684.2:g.19895474G>C	GRCh38
NC_000022.10:g.19882997G>C , CM000684.1:g.19882997G>C	GRCh37
NC_000022.9:g.18262997G>C	NCBI36
NG_011835.1:g.51363C>G , LRG_417:g.51363C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.882C>G MANE Select	ENSP00000383365.1:p.Val294=
ENST00000334363.14:c.882C>G	ENSP00000334451.9:p.Val294=
ENST00000400518.5:c.792C>G	ENSP00000383362.1:p.Val264=
ENST00000400519.6:c.879C>G	ENSP00000383363.1:p.Val293=
ENST00000400521.6:c.882C>G	ENSP00000383365.1:p.Val294=
ENST00000400525.6:c.813C>G	ENSP00000383369.3:p.Val271=
ENST00000474308.5:c.825C>G	ENSP00000485665.1:p.Val275=
ENST00000475995.3:c.379C>G
ENST00000491939.6:c.786C>G	ENSP00000485543.1:p.Val262=
ENST00000494454.5:n.956C>G
ENST00000542719.6:c.594C>G	ENSP00000485128.2:p.Val198=
ENST00000634537.1:c.111C>G	ENSP00000489208.1:p.Val37=
ENST00000635155.1:n.468C>G
NM_001282512.1:c.882C>G	NP_001269441.1:p.Val294=
NM_006440.4:c.882C>G	NP_006431.2:p.Val294=
NM_001282512.2:c.882C>G	NP_001269441.1:p.Val294=
NM_001352300.1:c.879C>G	NP_001339229.1:p.Val293=
NM_001352301.1:c.792C>G	NP_001339230.1:p.Val264=
NM_001352302.1:c.594C>G	NP_001339231.1:p.Val198=
NM_001352303.1:c.786C>G	NP_001339232.1:p.Val262=
NR_147957.1:n.1014C>G
NM_006440.5:c.882C>G MANE Select	NP_006431.2:p.Val294=
NM_001282512.3:c.882C>G	NP_001269441.1:p.Val294=
NM_001352300.2:c.879C>G	NP_001339229.1:p.Val293=
NR_147957.2:n.840C>G
NM_001352301.2:c.792C>G	NP_001339230.1:p.Val264=
NM_001352302.2:c.594C>G	NP_001339231.1:p.Val198=
NM_001352303.2:c.786C>G	NP_001339232.1:p.Val262=