Canonical Allele Identifier: CA2396091984

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895498C= , CM000684.2:g.19895498C=	GRCh38
NC_000022.10:g.19883021C= , CM000684.1:g.19883021C=	GRCh37
NC_000022.9:g.18263021C=	NCBI36
NG_011835.1:g.51339G= , LRG_417:g.51339G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.858G= MANE Select	ENSP00000383365.1:p.Arg286=
ENST00000334363.14:c.858G=	ENSP00000334451.9:p.Arg286=
ENST00000400518.5:c.768G=	ENSP00000383362.1:p.Arg256=
ENST00000400519.6:c.855G=	ENSP00000383363.1:p.Arg285=
ENST00000400521.6:c.858G=	ENSP00000383365.1:p.Arg286=
ENST00000400525.6:c.789G=	ENSP00000383369.3:p.Arg263=
ENST00000474308.5:c.801G=	ENSP00000485665.1:p.Arg267=
ENST00000475995.3:c.355G=
ENST00000491939.6:c.762G=	ENSP00000485543.1:p.Arg254=
ENST00000494454.5:n.932G=
ENST00000542719.6:c.570G=	ENSP00000485128.2:p.Arg190=
ENST00000634537.1:c.87G=	ENSP00000489208.1:p.Arg29=
ENST00000635155.1:n.444G=
NM_001282512.1:c.858G=	NP_001269441.1:p.Arg286=
NM_006440.4:c.858G=	NP_006431.2:p.Arg286=
NM_001282512.2:c.858G=	NP_001269441.1:p.Arg286=
NM_001352300.1:c.855G=	NP_001339229.1:p.Arg285=
NM_001352301.1:c.768G=	NP_001339230.1:p.Arg256=
NM_001352302.1:c.570G=	NP_001339231.1:p.Arg190=
NM_001352303.1:c.762G=	NP_001339232.1:p.Arg254=
NR_147957.1:n.990G=
NM_006440.5:c.858G= MANE Select	NP_006431.2:p.Arg286=
NM_001282512.3:c.858G=	NP_001269441.1:p.Arg286=
NM_001352300.2:c.855G=	NP_001339229.1:p.Arg285=
NR_147957.2:n.816G=
NM_001352301.2:c.768G=	NP_001339230.1:p.Arg256=
NM_001352302.2:c.570G=	NP_001339231.1:p.Arg190=
NM_001352303.2:c.762G=	NP_001339232.1:p.Arg254=