Canonical Allele Identifier: CA2396103735

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918887T= , CM000684.2:g.19918887T=	GRCh38
NC_000022.10:g.19906410T= , CM000684.1:g.19906410T=	GRCh37
NC_000022.9:g.18286410T=	NCBI36
NG_011835.1:g.27950A= , LRG_417:g.27950A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.347A= MANE Select	ENSP00000383365.1:p.Glu116=
ENST00000334363.14:c.347A=	ENSP00000334451.9:p.Glu116=
ENST00000400518.5:c.257A=	ENSP00000383362.1:p.Glu86=
ENST00000400519.6:c.344A=	ENSP00000383363.1:p.Glu115=
ENST00000400521.6:c.347A=	ENSP00000383365.1:p.Glu116=
ENST00000400525.6:c.278A=	ENSP00000383369.3:p.Glu93=
ENST00000474308.5:c.290A=	ENSP00000485665.1:p.Glu97=
ENST00000491939.6:c.251A=	ENSP00000485543.1:p.Glu84=
ENST00000496729.2:n.352A=
ENST00000542719.6:c.59A=	ENSP00000485128.2:p.Glu20=
NM_001282512.1:c.347A=	NP_001269441.1:p.Glu116=
NM_006440.4:c.347A=	NP_006431.2:p.Glu116=
NM_001282512.2:c.347A=	NP_001269441.1:p.Glu116=
NM_001352300.1:c.344A=	NP_001339229.1:p.Glu115=
NM_001352301.1:c.257A=	NP_001339230.1:p.Glu86=
NM_001352302.1:c.59A=	NP_001339231.1:p.Glu20=
NM_001352303.1:c.251A=	NP_001339232.1:p.Glu84=
NR_147957.1:n.479A=
NM_006440.5:c.347A= MANE Select	NP_006431.2:p.Glu116=
NM_001282512.3:c.347A=	NP_001269441.1:p.Glu116=
NM_001352300.2:c.344A=	NP_001339229.1:p.Glu115=
NR_147957.2:n.305A=
NM_001352301.2:c.257A=	NP_001339230.1:p.Glu86=
NM_001352302.2:c.59A=	NP_001339231.1:p.Glu20=
NM_001352303.2:c.251A=	NP_001339232.1:p.Glu84=