Canonical Allele Identifier: CA2396103774

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918961G= , CM000684.2:g.19918961G=	GRCh38
NC_000022.10:g.19906484G= , CM000684.1:g.19906484G=	GRCh37
NC_000022.9:g.18286484G=	NCBI36
NG_011835.1:g.27876C= , LRG_417:g.27876C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.273C= MANE Select	ENSP00000383365.1:p.Cys91=
ENST00000334363.14:c.273C=	ENSP00000334451.9:p.Cys91=
ENST00000400518.5:c.183C=	ENSP00000383362.1:p.Cys61=
ENST00000400519.6:c.270C=	ENSP00000383363.1:p.Cys90=
ENST00000400521.6:c.273C=	ENSP00000383365.1:p.Cys91=
ENST00000400525.6:c.204C=	ENSP00000383369.3:p.Cys68=
ENST00000474308.5:c.216C=	ENSP00000485665.1:p.Cys72=
ENST00000491939.6:c.177C=	ENSP00000485543.1:p.Cys59=
ENST00000496729.2:n.278C=
ENST00000542719.6:c.-16C=	ENSP00000485128.2:n.-16C=
NM_001282512.1:c.273C=	NP_001269441.1:p.Cys91=
NM_006440.4:c.273C=	NP_006431.2:p.Cys91=
NM_001282512.2:c.273C=	NP_001269441.1:p.Cys91=
NM_001352300.1:c.270C=	NP_001339229.1:p.Cys90=
NM_001352301.1:c.183C=	NP_001339230.1:p.Cys61=
NM_001352302.1:c.-16C=	NP_001339231.1:n.-16C=
NM_001352303.1:c.177C=	NP_001339232.1:p.Cys59=
NR_147957.1:n.405C=
NM_006440.5:c.273C= MANE Select	NP_006431.2:p.Cys91=
NM_001282512.3:c.273C=	NP_001269441.1:p.Cys91=
NM_001352300.2:c.270C=	NP_001339229.1:p.Cys90=
NR_147957.2:n.231C=
NM_001352301.2:c.183C=	NP_001339230.1:p.Cys61=
NM_001352302.2:c.-16C=	NP_001339231.1:n.-16C=
NM_001352303.2:c.177C=	NP_001339232.1:p.Cys59=