Canonical Allele Identifier: CA2396103723

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918870G= , CM000684.2:g.19918870G=	GRCh38
NC_000022.10:g.19906393G= , CM000684.1:g.19906393G=	GRCh37
NC_000022.9:g.18286393G=	NCBI36
NG_011835.1:g.27967C= , LRG_417:g.27967C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.364C= MANE Select	ENSP00000383365.1:p.Pro122=
ENST00000334363.14:c.364C=	ENSP00000334451.9:p.Pro122=
ENST00000400518.5:c.274C=	ENSP00000383362.1:p.Pro92=
ENST00000400519.6:c.361C=	ENSP00000383363.1:p.Pro121=
ENST00000400521.6:c.364C=	ENSP00000383365.1:p.Pro122=
ENST00000400525.6:c.295C=	ENSP00000383369.3:p.Pro99=
ENST00000474308.5:c.307C=	ENSP00000485665.1:p.Pro103=
ENST00000491939.6:c.268C=	ENSP00000485543.1:p.Pro90=
ENST00000496729.2:n.369C=
ENST00000542719.6:c.76C=	ENSP00000485128.2:p.Pro26=
NM_001282512.1:c.364C=	NP_001269441.1:p.Pro122=
NM_006440.4:c.364C=	NP_006431.2:p.Pro122=
NM_001282512.2:c.364C=	NP_001269441.1:p.Pro122=
NM_001352300.1:c.361C=	NP_001339229.1:p.Pro121=
NM_001352301.1:c.274C=	NP_001339230.1:p.Pro92=
NM_001352302.1:c.76C=	NP_001339231.1:p.Pro26=
NM_001352303.1:c.268C=	NP_001339232.1:p.Pro90=
NR_147957.1:n.496C=
NM_006440.5:c.364C= MANE Select	NP_006431.2:p.Pro122=
NM_001282512.3:c.364C=	NP_001269441.1:p.Pro122=
NM_001352300.2:c.361C=	NP_001339229.1:p.Pro121=
NR_147957.2:n.322C=
NM_001352301.2:c.274C=	NP_001339230.1:p.Pro92=
NM_001352302.2:c.76C=	NP_001339231.1:p.Pro26=
NM_001352303.2:c.268C=	NP_001339232.1:p.Pro90=