Canonical Allele Identifier: CA2396091960

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895439G= , CM000684.2:g.19895439G=	GRCh38
NC_000022.10:g.19882962G= , CM000684.1:g.19882962G=	GRCh37
NC_000022.9:g.18262962G=	NCBI36
NG_011835.1:g.51398C= , LRG_417:g.51398C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.917C= MANE Select	ENSP00000383365.1:p.Thr306=
ENST00000334363.14:c.917C=	ENSP00000334451.9:p.Thr306=
ENST00000400518.5:c.827C=	ENSP00000383362.1:p.Thr276=
ENST00000400519.6:c.914C=	ENSP00000383363.1:p.Thr305=
ENST00000400521.6:c.917C=	ENSP00000383365.1:p.Thr306=
ENST00000400525.6:c.848C=	ENSP00000383369.3:p.Thr283=
ENST00000474308.5:c.860C=	ENSP00000485665.1:p.Thr287=
ENST00000475995.3:c.414C=
ENST00000491939.6:c.821C=	ENSP00000485543.1:p.Thr274=
ENST00000494454.5:n.991C=
ENST00000542719.6:c.629C=	ENSP00000485128.2:p.Thr210=
ENST00000634537.1:c.146C=	ENSP00000489208.1:p.Thr49=
ENST00000635155.1:n.503C=
NM_001282512.1:c.917C=	NP_001269441.1:p.Thr306=
NM_006440.4:c.917C=	NP_006431.2:p.Thr306=
NM_001282512.2:c.917C=	NP_001269441.1:p.Thr306=
NM_001352300.1:c.914C=	NP_001339229.1:p.Thr305=
NM_001352301.1:c.827C=	NP_001339230.1:p.Thr276=
NM_001352302.1:c.629C=	NP_001339231.1:p.Thr210=
NM_001352303.1:c.821C=	NP_001339232.1:p.Thr274=
NR_147957.1:n.1049C=
NM_006440.5:c.917C= MANE Select	NP_006431.2:p.Thr306=
NM_001282512.3:c.917C=	NP_001269441.1:p.Thr306=
NM_001352300.2:c.914C=	NP_001339229.1:p.Thr305=
NR_147957.2:n.875C=
NM_001352301.2:c.827C=	NP_001339230.1:p.Thr276=
NM_001352302.2:c.629C=	NP_001339231.1:p.Thr210=
NM_001352303.2:c.821C=	NP_001339232.1:p.Thr274=