Canonical Allele Identifier: CA2396091981

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895491C= , CM000684.2:g.19895491C=	GRCh38
NC_000022.10:g.19883014C= , CM000684.1:g.19883014C=	GRCh37
NC_000022.9:g.18263014C=	NCBI36
NG_011835.1:g.51346G= , LRG_417:g.51346G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.865G= MANE Select	ENSP00000383365.1:p.Asp289=
ENST00000334363.14:c.865G=	ENSP00000334451.9:p.Asp289=
ENST00000400518.5:c.775G=	ENSP00000383362.1:p.Asp259=
ENST00000400519.6:c.862G=	ENSP00000383363.1:p.Asp288=
ENST00000400521.6:c.865G=	ENSP00000383365.1:p.Asp289=
ENST00000400525.6:c.796G=	ENSP00000383369.3:p.Asp266=
ENST00000474308.5:c.808G=	ENSP00000485665.1:p.Asp270=
ENST00000475995.3:c.362G=
ENST00000491939.6:c.769G=	ENSP00000485543.1:p.Asp257=
ENST00000494454.5:n.939G=
ENST00000542719.6:c.577G=	ENSP00000485128.2:p.Asp193=
ENST00000634537.1:c.94G=	ENSP00000489208.1:p.Asp32=
ENST00000635155.1:n.451G=
NM_001282512.1:c.865G=	NP_001269441.1:p.Asp289=
NM_006440.4:c.865G=	NP_006431.2:p.Asp289=
NM_001282512.2:c.865G=	NP_001269441.1:p.Asp289=
NM_001352300.1:c.862G=	NP_001339229.1:p.Asp288=
NM_001352301.1:c.775G=	NP_001339230.1:p.Asp259=
NM_001352302.1:c.577G=	NP_001339231.1:p.Asp193=
NM_001352303.1:c.769G=	NP_001339232.1:p.Asp257=
NR_147957.1:n.997G=
NM_006440.5:c.865G= MANE Select	NP_006431.2:p.Asp289=
NM_001282512.3:c.865G=	NP_001269441.1:p.Asp289=
NM_001352300.2:c.862G=	NP_001339229.1:p.Asp288=
NR_147957.2:n.823G=
NM_001352301.2:c.775G=	NP_001339230.1:p.Asp259=
NM_001352302.2:c.577G=	NP_001339231.1:p.Asp193=
NM_001352303.2:c.769G=	NP_001339232.1:p.Asp257=