Canonical Allele Identifier: CA513365442

Gene: TXNRD2

Linked Data

• COSMIC: COSM6311653 ; COSM6311654
• MyVariant Identifiers: chr22:g.19883063G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895540G>T , CM000684.2:g.19895540G>T	GRCh38
NC_000022.10:g.19883063G>T , CM000684.1:g.19883063G>T	GRCh37
NC_000022.9:g.18263063G>T	NCBI36
NG_011835.1:g.51297C>A , LRG_417:g.51297C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.816C>A MANE Select	ENSP00000383365.1:p.Gly272=
ENST00000334363.14:c.816C>A	ENSP00000334451.9:p.Gly272=
ENST00000400518.5:c.726C>A	ENSP00000383362.1:p.Gly242=
ENST00000400519.6:c.813C>A	ENSP00000383363.1:p.Gly271=
ENST00000400521.6:c.816C>A	ENSP00000383365.1:p.Gly272=
ENST00000400525.6:c.747C>A	ENSP00000383369.3:p.Gly249=
ENST00000474308.5:c.759C>A	ENSP00000485665.1:p.Gly253=
ENST00000475995.3:c.313C>A
ENST00000491939.6:c.720C>A	ENSP00000485543.1:p.Gly240=
ENST00000494454.5:n.890C>A
ENST00000542719.6:c.528C>A	ENSP00000485128.2:p.Gly176=
ENST00000634537.1:c.45C>A	ENSP00000489208.1:p.Gly15=
ENST00000635155.1:n.402C>A
NM_001282512.1:c.816C>A	NP_001269441.1:p.Gly272=
NM_006440.4:c.816C>A	NP_006431.2:p.Gly272=
NM_001282512.2:c.816C>A	NP_001269441.1:p.Gly272=
NM_001352300.1:c.813C>A	NP_001339229.1:p.Gly271=
NM_001352301.1:c.726C>A	NP_001339230.1:p.Gly242=
NM_001352302.1:c.528C>A	NP_001339231.1:p.Gly176=
NM_001352303.1:c.720C>A	NP_001339232.1:p.Gly240=
NR_147957.1:n.948C>A
NM_006440.5:c.816C>A MANE Select	NP_006431.2:p.Gly272=
NM_001282512.3:c.816C>A	NP_001269441.1:p.Gly272=
NM_001352300.2:c.813C>A	NP_001339229.1:p.Gly271=
NR_147957.2:n.774C>A
NM_001352301.2:c.726C>A	NP_001339230.1:p.Gly242=
NM_001352302.2:c.528C>A	NP_001339231.1:p.Gly176=
NM_001352303.2:c.720C>A	NP_001339232.1:p.Gly240=