Canonical Allele Identifier: CA2396104134

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19919576C= , CM000684.2:g.19919576C=	GRCh38
NC_000022.10:g.19907099C= , CM000684.1:g.19907099C=	GRCh37
NC_000022.9:g.18287099C=	NCBI36
NG_011835.1:g.27261G= , LRG_417:g.27261G=

Transcript Alleles

HGVS	Amino-acid Change
NM_006440.5:c.196G= MANE Select	NP_006431.2:p.Ala66=
ENST00000400521.7:c.196G= MANE Select	ENSP00000383365.1:p.Ala66=
NM_001282512.1:c.196G=	NP_001269441.1:p.Ala66=
NM_001282512.2:c.196G=	NP_001269441.1:p.Ala66=
NM_001282512.3:c.196G=	NP_001269441.1:p.Ala66=
NM_001352300.1:c.193G=	NP_001339229.1:p.Ala65=
NM_001352300.2:c.193G=	NP_001339229.1:p.Ala65=
NM_001352301.1:c.106G=	NP_001339230.1:p.Ala36=
NM_001352301.2:c.106G=	NP_001339230.1:p.Ala36=
NM_001352302.1:c.-93G=	NP_001339231.1:n.-93G=
NM_001352302.2:c.-93G=	NP_001339231.1:n.-93G=
NM_001352303.1:c.100G=	NP_001339232.1:p.Ala34=
NM_001352303.2:c.100G=	NP_001339232.1:p.Ala34=
NM_006440.4:c.196G=	NP_006431.2:p.Ala66=
NR_147957.1:n.362-572G=
NR_147957.2:n.188-572G=
ENST00000334363.14:c.196G=	ENSP00000334451.9:p.Ala66=
ENST00000400518.5:c.106G=	ENSP00000383362.1:p.Ala36=
ENST00000400519.6:c.193G=	ENSP00000383363.1:p.Ala65=
ENST00000400521.6:c.196G=	ENSP00000383365.1:p.Ala66=
ENST00000400525.6:c.127G=	ENSP00000383369.3:p.Ala43=
ENST00000474308.5:c.173-572G=	ENSP00000485665.1:n.173-572G=
ENST00000491939.6:c.100G=	ENSP00000485543.1:p.Ala34=
ENST00000496729.2:n.201G=
ENST00000542719.6:c.-93G=	ENSP00000485128.2:n.-93G=