Canonical Allele Identifier: CA2396103775

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918962C= , CM000684.2:g.19918962C=	GRCh38
NC_000022.10:g.19906485C= , CM000684.1:g.19906485C=	GRCh37
NC_000022.9:g.18286485C=	NCBI36
NG_011835.1:g.27875G= , LRG_417:g.27875G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.272G= MANE Select	ENSP00000383365.1:p.Cys91=
ENST00000334363.14:c.272G=	ENSP00000334451.9:p.Cys91=
ENST00000400518.5:c.182G=	ENSP00000383362.1:p.Cys61=
ENST00000400519.6:c.269G=	ENSP00000383363.1:p.Cys90=
ENST00000400521.6:c.272G=	ENSP00000383365.1:p.Cys91=
ENST00000400525.6:c.203G=	ENSP00000383369.3:p.Cys68=
ENST00000474308.5:c.215G=	ENSP00000485665.1:p.Cys72=
ENST00000491939.6:c.176G=	ENSP00000485543.1:p.Cys59=
ENST00000496729.2:n.277G=
ENST00000542719.6:c.-17G=	ENSP00000485128.2:n.-17G=
NM_001282512.1:c.272G=	NP_001269441.1:p.Cys91=
NM_006440.4:c.272G=	NP_006431.2:p.Cys91=
NM_001282512.2:c.272G=	NP_001269441.1:p.Cys91=
NM_001352300.1:c.269G=	NP_001339229.1:p.Cys90=
NM_001352301.1:c.182G=	NP_001339230.1:p.Cys61=
NM_001352302.1:c.-17G=	NP_001339231.1:n.-17G=
NM_001352303.1:c.176G=	NP_001339232.1:p.Cys59=
NR_147957.1:n.404G=
NM_006440.5:c.272G= MANE Select	NP_006431.2:p.Cys91=
NM_001282512.3:c.272G=	NP_001269441.1:p.Cys91=
NM_001352300.2:c.269G=	NP_001339229.1:p.Cys90=
NR_147957.2:n.230G=
NM_001352301.2:c.182G=	NP_001339230.1:p.Cys61=
NM_001352302.2:c.-17G=	NP_001339231.1:n.-17G=
NM_001352303.2:c.176G=	NP_001339232.1:p.Cys59=