Canonical Allele Identifier: CA2396092010

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895560C= , CM000684.2:g.19895560C=	GRCh38
NC_000022.10:g.19883083C= , CM000684.1:g.19883083C=	GRCh37
NC_000022.9:g.18263083C=	NCBI36
NG_011835.1:g.51277G= , LRG_417:g.51277G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.796G= MANE Select	ENSP00000383365.1:p.Glu266=
ENST00000334363.14:c.796G=	ENSP00000334451.9:p.Glu266=
ENST00000400518.5:c.706G=	ENSP00000383362.1:p.Glu236=
ENST00000400519.6:c.793G=	ENSP00000383363.1:p.Glu265=
ENST00000400521.6:c.796G=	ENSP00000383365.1:p.Glu266=
ENST00000400525.6:c.727G=	ENSP00000383369.3:p.Glu243=
ENST00000474308.5:c.739G=	ENSP00000485665.1:p.Glu247=
ENST00000475995.3:c.293G=
ENST00000491939.6:c.700G=	ENSP00000485543.1:p.Glu234=
ENST00000494454.5:n.870G=
ENST00000542719.6:c.508G=	ENSP00000485128.2:p.Glu170=
ENST00000634537.1:c.25G=	ENSP00000489208.1:p.Glu9=
ENST00000635155.1:n.382G=
NM_001282512.1:c.796G=	NP_001269441.1:p.Glu266=
NM_006440.4:c.796G=	NP_006431.2:p.Glu266=
NM_001282512.2:c.796G=	NP_001269441.1:p.Glu266=
NM_001352300.1:c.793G=	NP_001339229.1:p.Glu265=
NM_001352301.1:c.706G=	NP_001339230.1:p.Glu236=
NM_001352302.1:c.508G=	NP_001339231.1:p.Glu170=
NM_001352303.1:c.700G=	NP_001339232.1:p.Glu234=
NR_147957.1:n.928G=
NM_006440.5:c.796G= MANE Select	NP_006431.2:p.Glu266=
NM_001282512.3:c.796G=	NP_001269441.1:p.Glu266=
NM_001352300.2:c.793G=	NP_001339229.1:p.Glu265=
NR_147957.2:n.754G=
NM_001352301.2:c.706G=	NP_001339230.1:p.Glu236=
NM_001352302.2:c.508G=	NP_001339231.1:p.Glu170=
NM_001352303.2:c.700G=	NP_001339232.1:p.Glu234=