Canonical Allele Identifier: CA2396084862

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880682G= , CM000684.2:g.19880682G=	GRCh38
NC_000022.10:g.19868205G= , CM000684.1:g.19868205G=	GRCh37
NC_000022.9:g.18248205G=	NCBI36
NG_011835.1:g.66155C= , LRG_417:g.66155C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1122C= MANE Select	ENSP00000383365.1:p.Ala374=
ENST00000400518.5:c.1032C=	ENSP00000383362.1:p.Ala344=
ENST00000400519.6:c.1119C=	ENSP00000383363.1:p.Ala373=
ENST00000400521.6:c.1122C=	ENSP00000383365.1:p.Ala374=
ENST00000400525.6:c.1053C=	ENSP00000383369.3:p.Ala351=
ENST00000462330.5:c.45C=	ENSP00000485603.2:p.Ala15=
ENST00000462843.2:c.72C=	ENSP00000485466.2:p.Ala24=
ENST00000474308.5:c.1065C=	ENSP00000485665.1:p.Ala355=
ENST00000485358.5:c.90C=	ENSP00000485499.2:p.Ala30=
ENST00000487165.5:n.1216C=
ENST00000494454.5:n.1196C=
ENST00000495655.2:n.666C=
ENST00000542719.6:c.834C=	ENSP00000485128.2:p.Ala278=
ENST00000634471.1:n.244-411C=
ENST00000634537.1:c.351C=	ENSP00000489208.1:p.Ala117=
NM_006440.4:c.1122C=	NP_006431.2:p.Ala374=
NM_001352300.1:c.1119C=	NP_001339229.1:p.Ala373=
NM_001352301.1:c.1032C=	NP_001339230.1:p.Ala344=
NM_001352302.1:c.834C=	NP_001339231.1:p.Ala278=
NR_147957.1:n.1254C=
NM_006440.5:c.1122C= MANE Select	NP_006431.2:p.Ala374=
NM_001352300.2:c.1119C=	NP_001339229.1:p.Ala373=
NR_147957.2:n.1080C=
NM_001352301.2:c.1032C=	NP_001339230.1:p.Ala344=
NM_001352302.2:c.834C=	NP_001339231.1:p.Ala278=