Canonical Allele Identifier: CA2396103769

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918952C= , CM000684.2:g.19918952C=	GRCh38
NC_000022.10:g.19906475C= , CM000684.1:g.19906475C=	GRCh37
NC_000022.9:g.18286475C=	NCBI36
NG_011835.1:g.27885G= , LRG_417:g.27885G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.282G= MANE Select	ENSP00000383365.1:p.Lys94=
ENST00000334363.14:c.282G=	ENSP00000334451.9:p.Lys94=
ENST00000400518.5:c.192G=	ENSP00000383362.1:p.Lys64=
ENST00000400519.6:c.279G=	ENSP00000383363.1:p.Lys93=
ENST00000400521.6:c.282G=	ENSP00000383365.1:p.Lys94=
ENST00000400525.6:c.213G=	ENSP00000383369.3:p.Lys71=
ENST00000474308.5:c.225G=	ENSP00000485665.1:p.Lys75=
ENST00000491939.6:c.186G=	ENSP00000485543.1:p.Lys62=
ENST00000496729.2:n.287G=
ENST00000542719.6:c.-7G=	ENSP00000485128.2:n.-7G=
NM_001282512.1:c.282G=	NP_001269441.1:p.Lys94=
NM_006440.4:c.282G=	NP_006431.2:p.Lys94=
NM_001282512.2:c.282G=	NP_001269441.1:p.Lys94=
NM_001352300.1:c.279G=	NP_001339229.1:p.Lys93=
NM_001352301.1:c.192G=	NP_001339230.1:p.Lys64=
NM_001352302.1:c.-7G=	NP_001339231.1:n.-7G=
NM_001352303.1:c.186G=	NP_001339232.1:p.Lys62=
NR_147957.1:n.414G=
NM_006440.5:c.282G= MANE Select	NP_006431.2:p.Lys94=
NM_001282512.3:c.282G=	NP_001269441.1:p.Lys94=
NM_001352300.2:c.279G=	NP_001339229.1:p.Lys93=
NR_147957.2:n.240G=
NM_001352301.2:c.192G=	NP_001339230.1:p.Lys64=
NM_001352302.2:c.-7G=	NP_001339231.1:n.-7G=
NM_001352303.2:c.186G=	NP_001339232.1:p.Lys62=