Canonical Allele Identifier: CA2396103777

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918965C= , CM000684.2:g.19918965C=	GRCh38
NC_000022.10:g.19906488C= , CM000684.1:g.19906488C=	GRCh37
NC_000022.9:g.18286488C=	NCBI36
NG_011835.1:g.27872G= , LRG_417:g.27872G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.269G= MANE Select	ENSP00000383365.1:p.Gly90=
ENST00000334363.14:c.269G=	ENSP00000334451.9:p.Gly90=
ENST00000400518.5:c.179G=	ENSP00000383362.1:p.Gly60=
ENST00000400519.6:c.266G=	ENSP00000383363.1:p.Gly89=
ENST00000400521.6:c.269G=	ENSP00000383365.1:p.Gly90=
ENST00000400525.6:c.200G=	ENSP00000383369.3:p.Gly67=
ENST00000474308.5:c.212G=	ENSP00000485665.1:p.Gly71=
ENST00000491939.6:c.173G=	ENSP00000485543.1:p.Gly58=
ENST00000496729.2:n.274G=
ENST00000542719.6:c.-20G=	ENSP00000485128.2:n.-20G=
NM_001282512.1:c.269G=	NP_001269441.1:p.Gly90=
NM_006440.4:c.269G=	NP_006431.2:p.Gly90=
NM_001282512.2:c.269G=	NP_001269441.1:p.Gly90=
NM_001352300.1:c.266G=	NP_001339229.1:p.Gly89=
NM_001352301.1:c.179G=	NP_001339230.1:p.Gly60=
NM_001352302.1:c.-20G=	NP_001339231.1:n.-20G=
NM_001352303.1:c.173G=	NP_001339232.1:p.Gly58=
NR_147957.1:n.401G=
NM_006440.5:c.269G= MANE Select	NP_006431.2:p.Gly90=
NM_001282512.3:c.269G=	NP_001269441.1:p.Gly90=
NM_001352300.2:c.266G=	NP_001339229.1:p.Gly89=
NR_147957.2:n.227G=
NM_001352301.2:c.179G=	NP_001339230.1:p.Gly60=
NM_001352302.2:c.-20G=	NP_001339231.1:n.-20G=
NM_001352303.2:c.173G=	NP_001339232.1:p.Gly58=