Canonical Allele Identifier: CA2396091964

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895453G= , CM000684.2:g.19895453G=	GRCh38
NC_000022.10:g.19882976G= , CM000684.1:g.19882976G=	GRCh37
NC_000022.9:g.18262976G=	NCBI36
NG_011835.1:g.51384C= , LRG_417:g.51384C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.903C= MANE Select	ENSP00000383365.1:p.Thr301=
ENST00000334363.14:c.903C=	ENSP00000334451.9:p.Thr301=
ENST00000400518.5:c.813C=	ENSP00000383362.1:p.Thr271=
ENST00000400519.6:c.900C=	ENSP00000383363.1:p.Thr300=
ENST00000400521.6:c.903C=	ENSP00000383365.1:p.Thr301=
ENST00000400525.6:c.834C=	ENSP00000383369.3:p.Thr278=
ENST00000474308.5:c.846C=	ENSP00000485665.1:p.Thr282=
ENST00000475995.3:c.400C=
ENST00000491939.6:c.807C=	ENSP00000485543.1:p.Thr269=
ENST00000494454.5:n.977C=
ENST00000542719.6:c.615C=	ENSP00000485128.2:p.Thr205=
ENST00000634537.1:c.132C=	ENSP00000489208.1:p.Thr44=
ENST00000635155.1:n.489C=
NM_001282512.1:c.903C=	NP_001269441.1:p.Thr301=
NM_006440.4:c.903C=	NP_006431.2:p.Thr301=
NM_001282512.2:c.903C=	NP_001269441.1:p.Thr301=
NM_001352300.1:c.900C=	NP_001339229.1:p.Thr300=
NM_001352301.1:c.813C=	NP_001339230.1:p.Thr271=
NM_001352302.1:c.615C=	NP_001339231.1:p.Thr205=
NM_001352303.1:c.807C=	NP_001339232.1:p.Thr269=
NR_147957.1:n.1035C=
NM_006440.5:c.903C= MANE Select	NP_006431.2:p.Thr301=
NM_001282512.3:c.903C=	NP_001269441.1:p.Thr301=
NM_001352300.2:c.900C=	NP_001339229.1:p.Thr300=
NR_147957.2:n.861C=
NM_001352301.2:c.813C=	NP_001339230.1:p.Thr271=
NM_001352302.2:c.615C=	NP_001339231.1:p.Thr205=
NM_001352303.2:c.807C=	NP_001339232.1:p.Thr269=