Canonical Allele Identifier: CA2396091807

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895143C= , CM000684.2:g.19895143C=	GRCh38
NC_000022.10:g.19882666C= , CM000684.1:g.19882666C=	GRCh37
NC_000022.9:g.18262666C=	NCBI36
NG_011835.1:g.51694G= , LRG_417:g.51694G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.949+264G= MANE Select	ENSP00000383365.1:n.949+264G=
ENST00000334363.14:c.1007G=	ENSP00000334451.9:p.Arg336=
ENST00000400518.5:c.859+264G=	ENSP00000383362.1:n.859+264G=
ENST00000400519.6:c.946+264G=	ENSP00000383363.1:n.946+264G=
ENST00000400521.6:c.949+264G=	ENSP00000383365.1:n.949+264G=
ENST00000400525.6:c.880+264G=	ENSP00000383369.3:n.880+264G=
ENST00000474308.5:c.892+264G=	ENSP00000485665.1:n.892+264G=
ENST00000475995.3:c.624G=
ENST00000491939.6:c.911G=	ENSP00000485543.1:p.Arg304=
ENST00000494454.5:n.1023+264G=
ENST00000542719.6:c.661+264G=	ENSP00000485128.2:n.661+264G=
ENST00000634537.1:c.178+264G=	ENSP00000489208.1:n.178+264G=
ENST00000635155.1:n.535+264G=
NM_001282512.1:c.1007G=	NP_001269441.1:p.Arg336=
NM_006440.4:c.949+264G=	NP_006431.2:n.949+264G=
NM_001282512.2:c.1007G=	NP_001269441.1:p.Arg336=
NM_001352300.1:c.946+264G=	NP_001339229.1:n.946+264G=
NM_001352301.1:c.859+264G=	NP_001339230.1:n.859+264G=
NM_001352302.1:c.661+264G=	NP_001339231.1:n.661+264G=
NM_001352303.1:c.911G=	NP_001339232.1:p.Arg304=
NR_147957.1:n.1081+264G=
NM_006440.5:c.949+264G= MANE Select	NP_006431.2:n.949+264G=
NM_001282512.3:c.1007G=	NP_001269441.1:p.Arg336=
NM_001352300.2:c.946+264G=	NP_001339229.1:n.946+264G=
NR_147957.2:n.907+264G=
NM_001352301.2:c.859+264G=	NP_001339230.1:n.859+264G=
NM_001352302.2:c.661+264G=	NP_001339231.1:n.661+264G=
NM_001352303.2:c.911G=	NP_001339232.1:p.Arg304=