Canonical Allele Identifier: CA2396103744

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918909C= , CM000684.2:g.19918909C=	GRCh38
NC_000022.10:g.19906432C= , CM000684.1:g.19906432C=	GRCh37
NC_000022.9:g.18286432C=	NCBI36
NG_011835.1:g.27928G= , LRG_417:g.27928G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.325G= MANE Select	ENSP00000383365.1:p.Asp109=
ENST00000334363.14:c.325G=	ENSP00000334451.9:p.Asp109=
ENST00000400518.5:c.235G=	ENSP00000383362.1:p.Asp79=
ENST00000400519.6:c.322G=	ENSP00000383363.1:p.Asp108=
ENST00000400521.6:c.325G=	ENSP00000383365.1:p.Asp109=
ENST00000400525.6:c.256G=	ENSP00000383369.3:p.Asp86=
ENST00000474308.5:c.268G=	ENSP00000485665.1:p.Asp90=
ENST00000491939.6:c.229G=	ENSP00000485543.1:p.Asp77=
ENST00000496729.2:n.330G=
ENST00000542719.6:c.37G=	ENSP00000485128.2:p.Asp13=
NM_001282512.1:c.325G=	NP_001269441.1:p.Asp109=
NM_006440.4:c.325G=	NP_006431.2:p.Asp109=
NM_001282512.2:c.325G=	NP_001269441.1:p.Asp109=
NM_001352300.1:c.322G=	NP_001339229.1:p.Asp108=
NM_001352301.1:c.235G=	NP_001339230.1:p.Asp79=
NM_001352302.1:c.37G=	NP_001339231.1:p.Asp13=
NM_001352303.1:c.229G=	NP_001339232.1:p.Asp77=
NR_147957.1:n.457G=
NM_006440.5:c.325G= MANE Select	NP_006431.2:p.Asp109=
NM_001282512.3:c.325G=	NP_001269441.1:p.Asp109=
NM_001352300.2:c.322G=	NP_001339229.1:p.Asp108=
NR_147957.2:n.283G=
NM_001352301.2:c.235G=	NP_001339230.1:p.Asp79=
NM_001352302.2:c.37G=	NP_001339231.1:p.Asp13=
NM_001352303.2:c.229G=	NP_001339232.1:p.Asp77=