Canonical Allele Identifier: CA2396103760

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918932G= , CM000684.2:g.19918932G=	GRCh38
NC_000022.10:g.19906455G= , CM000684.1:g.19906455G=	GRCh37
NC_000022.9:g.18286455G=	NCBI36
NG_011835.1:g.27905C= , LRG_417:g.27905C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.302C= MANE Select	ENSP00000383365.1:p.Ala101=
ENST00000334363.14:c.302C=	ENSP00000334451.9:p.Ala101=
ENST00000400518.5:c.212C=	ENSP00000383362.1:p.Ala71=
ENST00000400519.6:c.299C=	ENSP00000383363.1:p.Ala100=
ENST00000400521.6:c.302C=	ENSP00000383365.1:p.Ala101=
ENST00000400525.6:c.233C=	ENSP00000383369.3:p.Ala78=
ENST00000474308.5:c.245C=	ENSP00000485665.1:p.Ala82=
ENST00000491939.6:c.206C=	ENSP00000485543.1:p.Ala69=
ENST00000496729.2:n.307C=
ENST00000542719.6:c.14C=	ENSP00000485128.2:p.Ala5=
NM_001282512.1:c.302C=	NP_001269441.1:p.Ala101=
NM_006440.4:c.302C=	NP_006431.2:p.Ala101=
NM_001282512.2:c.302C=	NP_001269441.1:p.Ala101=
NM_001352300.1:c.299C=	NP_001339229.1:p.Ala100=
NM_001352301.1:c.212C=	NP_001339230.1:p.Ala71=
NM_001352302.1:c.14C=	NP_001339231.1:p.Ala5=
NM_001352303.1:c.206C=	NP_001339232.1:p.Ala69=
NR_147957.1:n.434C=
NM_006440.5:c.302C= MANE Select	NP_006431.2:p.Ala101=
NM_001282512.3:c.302C=	NP_001269441.1:p.Ala101=
NM_001352300.2:c.299C=	NP_001339229.1:p.Ala100=
NR_147957.2:n.260C=
NM_001352301.2:c.212C=	NP_001339230.1:p.Ala71=
NM_001352302.2:c.14C=	NP_001339231.1:p.Ala5=
NM_001352303.2:c.206C=	NP_001339232.1:p.Ala69=