Canonical Allele Identifier: CA2396084858

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880678T= , CM000684.2:g.19880678T=	GRCh38
NC_000022.10:g.19868201T= , CM000684.1:g.19868201T=	GRCh37
NC_000022.9:g.18248201T=	NCBI36
NG_011835.1:g.66159A= , LRG_417:g.66159A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1126A= MANE Select	ENSP00000383365.1:p.Arg376=
ENST00000400518.5:c.1036A=	ENSP00000383362.1:p.Arg346=
ENST00000400519.6:c.1123A=	ENSP00000383363.1:p.Arg375=
ENST00000400521.6:c.1126A=	ENSP00000383365.1:p.Arg376=
ENST00000400525.6:c.1057A=	ENSP00000383369.3:p.Arg353=
ENST00000462330.5:c.49A=	ENSP00000485603.2:p.Arg17=
ENST00000462843.2:c.76A=	ENSP00000485466.2:p.Arg26=
ENST00000474308.5:c.1069A=	ENSP00000485665.1:p.Arg357=
ENST00000485358.5:c.94A=	ENSP00000485499.2:p.Arg32=
ENST00000487165.5:n.1220A=
ENST00000494454.5:n.1200A=
ENST00000495655.2:n.670A=
ENST00000542719.6:c.838A=	ENSP00000485128.2:p.Arg280=
ENST00000634471.1:n.244-407A=
ENST00000634537.1:c.355A=	ENSP00000489208.1:p.Arg119=
NM_006440.4:c.1126A=	NP_006431.2:p.Arg376=
NM_001352300.1:c.1123A=	NP_001339229.1:p.Arg375=
NM_001352301.1:c.1036A=	NP_001339230.1:p.Arg346=
NM_001352302.1:c.838A=	NP_001339231.1:p.Arg280=
NR_147957.1:n.1258A=
NM_006440.5:c.1126A= MANE Select	NP_006431.2:p.Arg376=
NM_001352300.2:c.1123A=	NP_001339229.1:p.Arg375=
NR_147957.2:n.1084A=
NM_001352301.2:c.1036A=	NP_001339230.1:p.Arg346=
NM_001352302.2:c.838A=	NP_001339231.1:p.Arg280=