Canonical Allele Identifier: CA2396084847

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880662C= , CM000684.2:g.19880662C=	GRCh38
NC_000022.10:g.19868185C= , CM000684.1:g.19868185C=	GRCh37
NC_000022.9:g.18248185C=	NCBI36
NG_011835.1:g.66175G= , LRG_417:g.66175G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1142G= MANE Select	ENSP00000383365.1:p.Arg381=
ENST00000400518.5:c.1052G=	ENSP00000383362.1:p.Arg351=
ENST00000400519.6:c.1139G=	ENSP00000383363.1:p.Arg380=
ENST00000400521.6:c.1142G=	ENSP00000383365.1:p.Arg381=
ENST00000400525.6:c.1073G=	ENSP00000383369.3:p.Arg358=
ENST00000462330.5:c.65G=	ENSP00000485603.2:p.Arg22=
ENST00000462843.2:c.92G=	ENSP00000485466.2:p.Arg31=
ENST00000474308.5:c.1085G=	ENSP00000485665.1:p.Arg362=
ENST00000485358.5:c.110G=	ENSP00000485499.2:p.Arg37=
ENST00000487165.5:n.1236G=
ENST00000494454.5:n.1216G=
ENST00000495655.2:n.686G=
ENST00000542719.6:c.854G=	ENSP00000485128.2:p.Arg285=
ENST00000634471.1:n.244-391G=
ENST00000634537.1:c.371G=	ENSP00000489208.1:p.Arg124=
NM_006440.4:c.1142G=	NP_006431.2:p.Arg381=
NM_001352300.1:c.1139G=	NP_001339229.1:p.Arg380=
NM_001352301.1:c.1052G=	NP_001339230.1:p.Arg351=
NM_001352302.1:c.854G=	NP_001339231.1:p.Arg285=
NR_147957.1:n.1274G=
NM_006440.5:c.1142G= MANE Select	NP_006431.2:p.Arg381=
NM_001352300.2:c.1139G=	NP_001339229.1:p.Arg380=
NR_147957.2:n.1100G=
NM_001352301.2:c.1052G=	NP_001339230.1:p.Arg351=
NM_001352302.2:c.854G=	NP_001339231.1:p.Arg285=