Canonical Allele Identifier: CA2396091819

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895169G= , CM000684.2:g.19895169G=	GRCh38
NC_000022.10:g.19882692G= , CM000684.1:g.19882692G=	GRCh37
NC_000022.9:g.18262692G=	NCBI36
NG_011835.1:g.51668C= , LRG_417:g.51668C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.949+238C= MANE Select	ENSP00000383365.1:n.949+238C=
ENST00000334363.14:c.981C=	ENSP00000334451.9:p.Thr327=
ENST00000400518.5:c.859+238C=	ENSP00000383362.1:n.859+238C=
ENST00000400519.6:c.946+238C=	ENSP00000383363.1:n.946+238C=
ENST00000400521.6:c.949+238C=	ENSP00000383365.1:n.949+238C=
ENST00000400525.6:c.880+238C=	ENSP00000383369.3:n.880+238C=
ENST00000474308.5:c.892+238C=	ENSP00000485665.1:n.892+238C=
ENST00000475995.3:c.598C=
ENST00000491939.6:c.885C=	ENSP00000485543.1:p.Thr295=
ENST00000494454.5:n.1023+238C=
ENST00000542719.6:c.661+238C=	ENSP00000485128.2:n.661+238C=
ENST00000634537.1:c.178+238C=	ENSP00000489208.1:n.178+238C=
ENST00000635155.1:n.535+238C=
NM_001282512.1:c.981C=	NP_001269441.1:p.Thr327=
NM_006440.4:c.949+238C=	NP_006431.2:n.949+238C=
NM_001282512.2:c.981C=	NP_001269441.1:p.Thr327=
NM_001352300.1:c.946+238C=	NP_001339229.1:n.946+238C=
NM_001352301.1:c.859+238C=	NP_001339230.1:n.859+238C=
NM_001352302.1:c.661+238C=	NP_001339231.1:n.661+238C=
NM_001352303.1:c.885C=	NP_001339232.1:p.Thr295=
NR_147957.1:n.1081+238C=
NM_006440.5:c.949+238C= MANE Select	NP_006431.2:n.949+238C=
NM_001282512.3:c.981C=	NP_001269441.1:p.Thr327=
NM_001352300.2:c.946+238C=	NP_001339229.1:n.946+238C=
NR_147957.2:n.907+238C=
NM_001352301.2:c.859+238C=	NP_001339230.1:n.859+238C=
NM_001352302.2:c.661+238C=	NP_001339231.1:n.661+238C=
NM_001352303.2:c.885C=	NP_001339232.1:p.Thr295=