Canonical Allele Identifier: CA2396092009

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895557G= , CM000684.2:g.19895557G=	GRCh38
NC_000022.10:g.19883080G= , CM000684.1:g.19883080G=	GRCh37
NC_000022.9:g.18263080G=	NCBI36
NG_011835.1:g.51280C= , LRG_417:g.51280C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.799C= MANE Select	ENSP00000383365.1:p.His267=
ENST00000334363.14:c.799C=	ENSP00000334451.9:p.His267=
ENST00000400518.5:c.709C=	ENSP00000383362.1:p.His237=
ENST00000400519.6:c.796C=	ENSP00000383363.1:p.His266=
ENST00000400521.6:c.799C=	ENSP00000383365.1:p.His267=
ENST00000400525.6:c.730C=	ENSP00000383369.3:p.His244=
ENST00000474308.5:c.742C=	ENSP00000485665.1:p.His248=
ENST00000475995.3:c.296C=
ENST00000491939.6:c.703C=	ENSP00000485543.1:p.His235=
ENST00000494454.5:n.873C=
ENST00000542719.6:c.511C=	ENSP00000485128.2:p.His171=
ENST00000634537.1:c.28C=	ENSP00000489208.1:p.His10=
ENST00000635155.1:n.385C=
NM_001282512.1:c.799C=	NP_001269441.1:p.His267=
NM_006440.4:c.799C=	NP_006431.2:p.His267=
NM_001282512.2:c.799C=	NP_001269441.1:p.His267=
NM_001352300.1:c.796C=	NP_001339229.1:p.His266=
NM_001352301.1:c.709C=	NP_001339230.1:p.His237=
NM_001352302.1:c.511C=	NP_001339231.1:p.His171=
NM_001352303.1:c.703C=	NP_001339232.1:p.His235=
NR_147957.1:n.931C=
NM_006440.5:c.799C= MANE Select	NP_006431.2:p.His267=
NM_001282512.3:c.799C=	NP_001269441.1:p.His267=
NM_001352300.2:c.796C=	NP_001339229.1:p.His266=
NR_147957.2:n.757C=
NM_001352301.2:c.709C=	NP_001339230.1:p.His237=
NM_001352302.2:c.511C=	NP_001339231.1:p.His171=
NM_001352303.2:c.703C=	NP_001339232.1:p.His235=