Canonical Allele Identifier: CA2396092005

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895544T= , CM000684.2:g.19895544T=	GRCh38
NC_000022.10:g.19883067T= , CM000684.1:g.19883067T=	GRCh37
NC_000022.9:g.18263067T=	NCBI36
NG_011835.1:g.51293A= , LRG_417:g.51293A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.812A= MANE Select	ENSP00000383365.1:p.His271=
ENST00000334363.14:c.812A=	ENSP00000334451.9:p.His271=
ENST00000400518.5:c.722A=	ENSP00000383362.1:p.His241=
ENST00000400519.6:c.809A=	ENSP00000383363.1:p.His270=
ENST00000400521.6:c.812A=	ENSP00000383365.1:p.His271=
ENST00000400525.6:c.743A=	ENSP00000383369.3:p.His248=
ENST00000474308.5:c.755A=	ENSP00000485665.1:p.His252=
ENST00000475995.3:c.309A=
ENST00000491939.6:c.716A=	ENSP00000485543.1:p.His239=
ENST00000494454.5:n.886A=
ENST00000542719.6:c.524A=	ENSP00000485128.2:p.His175=
ENST00000634537.1:c.41A=	ENSP00000489208.1:p.His14=
ENST00000635155.1:n.398A=
NM_001282512.1:c.812A=	NP_001269441.1:p.His271=
NM_006440.4:c.812A=	NP_006431.2:p.His271=
NM_001282512.2:c.812A=	NP_001269441.1:p.His271=
NM_001352300.1:c.809A=	NP_001339229.1:p.His270=
NM_001352301.1:c.722A=	NP_001339230.1:p.His241=
NM_001352302.1:c.524A=	NP_001339231.1:p.His175=
NM_001352303.1:c.716A=	NP_001339232.1:p.His239=
NR_147957.1:n.944A=
NM_006440.5:c.812A= MANE Select	NP_006431.2:p.His271=
NM_001282512.3:c.812A=	NP_001269441.1:p.His271=
NM_001352300.2:c.809A=	NP_001339229.1:p.His270=
NR_147957.2:n.770A=
NM_001352301.2:c.722A=	NP_001339230.1:p.His241=
NM_001352302.2:c.524A=	NP_001339231.1:p.His175=
NM_001352303.2:c.716A=	NP_001339232.1:p.His239=