Canonical Allele Identifier: CA2396103751

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918920C= , CM000684.2:g.19918920C=	GRCh38
NC_000022.10:g.19906443C= , CM000684.1:g.19906443C=	GRCh37
NC_000022.9:g.18286443C=	NCBI36
NG_011835.1:g.27917G= , LRG_417:g.27917G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.314G= MANE Select	ENSP00000383365.1:p.Gly105=
ENST00000334363.14:c.314G=	ENSP00000334451.9:p.Gly105=
ENST00000400518.5:c.224G=	ENSP00000383362.1:p.Gly75=
ENST00000400519.6:c.311G=	ENSP00000383363.1:p.Gly104=
ENST00000400521.6:c.314G=	ENSP00000383365.1:p.Gly105=
ENST00000400525.6:c.245G=	ENSP00000383369.3:p.Gly82=
ENST00000474308.5:c.257G=	ENSP00000485665.1:p.Gly86=
ENST00000491939.6:c.218G=	ENSP00000485543.1:p.Gly73=
ENST00000496729.2:n.319G=
ENST00000542719.6:c.26G=	ENSP00000485128.2:p.Gly9=
NM_001282512.1:c.314G=	NP_001269441.1:p.Gly105=
NM_006440.4:c.314G=	NP_006431.2:p.Gly105=
NM_001282512.2:c.314G=	NP_001269441.1:p.Gly105=
NM_001352300.1:c.311G=	NP_001339229.1:p.Gly104=
NM_001352301.1:c.224G=	NP_001339230.1:p.Gly75=
NM_001352302.1:c.26G=	NP_001339231.1:p.Gly9=
NM_001352303.1:c.218G=	NP_001339232.1:p.Gly73=
NR_147957.1:n.446G=
NM_006440.5:c.314G= MANE Select	NP_006431.2:p.Gly105=
NM_001282512.3:c.314G=	NP_001269441.1:p.Gly105=
NM_001352300.2:c.311G=	NP_001339229.1:p.Gly104=
NR_147957.2:n.272G=
NM_001352301.2:c.224G=	NP_001339230.1:p.Gly75=
NM_001352302.2:c.26G=	NP_001339231.1:p.Gly9=
NM_001352303.2:c.218G=	NP_001339232.1:p.Gly73=