Canonical Allele Identifier: CA2396103737

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918890C= , CM000684.2:g.19918890C=	GRCh38
NC_000022.10:g.19906413C= , CM000684.1:g.19906413C=	GRCh37
NC_000022.9:g.18286413C=	NCBI36
NG_011835.1:g.27947G= , LRG_417:g.27947G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.344G= MANE Select	ENSP00000383365.1:p.Trp115=
ENST00000334363.14:c.344G=	ENSP00000334451.9:p.Trp115=
ENST00000400518.5:c.254G=	ENSP00000383362.1:p.Trp85=
ENST00000400519.6:c.341G=	ENSP00000383363.1:p.Trp114=
ENST00000400521.6:c.344G=	ENSP00000383365.1:p.Trp115=
ENST00000400525.6:c.275G=	ENSP00000383369.3:p.Trp92=
ENST00000474308.5:c.287G=	ENSP00000485665.1:p.Trp96=
ENST00000491939.6:c.248G=	ENSP00000485543.1:p.Trp83=
ENST00000496729.2:n.349G=
ENST00000542719.6:c.56G=	ENSP00000485128.2:p.Trp19=
NM_001282512.1:c.344G=	NP_001269441.1:p.Trp115=
NM_006440.4:c.344G=	NP_006431.2:p.Trp115=
NM_001282512.2:c.344G=	NP_001269441.1:p.Trp115=
NM_001352300.1:c.341G=	NP_001339229.1:p.Trp114=
NM_001352301.1:c.254G=	NP_001339230.1:p.Trp85=
NM_001352302.1:c.56G=	NP_001339231.1:p.Trp19=
NM_001352303.1:c.248G=	NP_001339232.1:p.Trp83=
NR_147957.1:n.476G=
NM_006440.5:c.344G= MANE Select	NP_006431.2:p.Trp115=
NM_001282512.3:c.344G=	NP_001269441.1:p.Trp115=
NM_001352300.2:c.341G=	NP_001339229.1:p.Trp114=
NR_147957.2:n.302G=
NM_001352301.2:c.254G=	NP_001339230.1:p.Trp85=
NM_001352302.2:c.56G=	NP_001339231.1:p.Trp19=
NM_001352303.2:c.248G=	NP_001339232.1:p.Trp83=