Canonical Allele Identifier: CA2396091999

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895534C= , CM000684.2:g.19895534C=	GRCh38
NC_000022.10:g.19883057C= , CM000684.1:g.19883057C=	GRCh37
NC_000022.9:g.18263057C=	NCBI36
NG_011835.1:g.51303G= , LRG_417:g.51303G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.822G= MANE Select	ENSP00000383365.1:p.Arg274=
ENST00000334363.14:c.822G=	ENSP00000334451.9:p.Arg274=
ENST00000400518.5:c.732G=	ENSP00000383362.1:p.Arg244=
ENST00000400519.6:c.819G=	ENSP00000383363.1:p.Arg273=
ENST00000400521.6:c.822G=	ENSP00000383365.1:p.Arg274=
ENST00000400525.6:c.753G=	ENSP00000383369.3:p.Arg251=
ENST00000474308.5:c.765G=	ENSP00000485665.1:p.Arg255=
ENST00000475995.3:c.319G=
ENST00000491939.6:c.726G=	ENSP00000485543.1:p.Arg242=
ENST00000494454.5:n.896G=
ENST00000542719.6:c.534G=	ENSP00000485128.2:p.Arg178=
ENST00000634537.1:c.51G=	ENSP00000489208.1:p.Arg17=
ENST00000635155.1:n.408G=
NM_001282512.1:c.822G=	NP_001269441.1:p.Arg274=
NM_006440.4:c.822G=	NP_006431.2:p.Arg274=
NM_001282512.2:c.822G=	NP_001269441.1:p.Arg274=
NM_001352300.1:c.819G=	NP_001339229.1:p.Arg273=
NM_001352301.1:c.732G=	NP_001339230.1:p.Arg244=
NM_001352302.1:c.534G=	NP_001339231.1:p.Arg178=
NM_001352303.1:c.726G=	NP_001339232.1:p.Arg242=
NR_147957.1:n.954G=
NM_006440.5:c.822G= MANE Select	NP_006431.2:p.Arg274=
NM_001282512.3:c.822G=	NP_001269441.1:p.Arg274=
NM_001352300.2:c.819G=	NP_001339229.1:p.Arg273=
NR_147957.2:n.780G=
NM_001352301.2:c.732G=	NP_001339230.1:p.Arg244=
NM_001352302.2:c.534G=	NP_001339231.1:p.Arg178=
NM_001352303.2:c.726G=	NP_001339232.1:p.Arg242=