Canonical Allele Identifier: CA2396092002

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895538G= , CM000684.2:g.19895538G=	GRCh38
NC_000022.10:g.19883061G= , CM000684.1:g.19883061G=	GRCh37
NC_000022.9:g.18263061G=	NCBI36
NG_011835.1:g.51299C= , LRG_417:g.51299C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.818C= MANE Select	ENSP00000383365.1:p.Thr273=
ENST00000334363.14:c.818C=	ENSP00000334451.9:p.Thr273=
ENST00000400518.5:c.728C=	ENSP00000383362.1:p.Thr243=
ENST00000400519.6:c.815C=	ENSP00000383363.1:p.Thr272=
ENST00000400521.6:c.818C=	ENSP00000383365.1:p.Thr273=
ENST00000400525.6:c.749C=	ENSP00000383369.3:p.Thr250=
ENST00000474308.5:c.761C=	ENSP00000485665.1:p.Thr254=
ENST00000475995.3:c.315C=
ENST00000491939.6:c.722C=	ENSP00000485543.1:p.Thr241=
ENST00000494454.5:n.892C=
ENST00000542719.6:c.530C=	ENSP00000485128.2:p.Thr177=
ENST00000634537.1:c.47C=	ENSP00000489208.1:p.Thr16=
ENST00000635155.1:n.404C=
NM_001282512.1:c.818C=	NP_001269441.1:p.Thr273=
NM_006440.4:c.818C=	NP_006431.2:p.Thr273=
NM_001282512.2:c.818C=	NP_001269441.1:p.Thr273=
NM_001352300.1:c.815C=	NP_001339229.1:p.Thr272=
NM_001352301.1:c.728C=	NP_001339230.1:p.Thr243=
NM_001352302.1:c.530C=	NP_001339231.1:p.Thr177=
NM_001352303.1:c.722C=	NP_001339232.1:p.Thr241=
NR_147957.1:n.950C=
NM_006440.5:c.818C= MANE Select	NP_006431.2:p.Thr273=
NM_001282512.3:c.818C=	NP_001269441.1:p.Thr273=
NM_001352300.2:c.815C=	NP_001339229.1:p.Thr272=
NR_147957.2:n.776C=
NM_001352301.2:c.728C=	NP_001339230.1:p.Thr243=
NM_001352302.2:c.530C=	NP_001339231.1:p.Thr177=
NM_001352303.2:c.722C=	NP_001339232.1:p.Thr241=