Canonical Allele Identifier: CA2396091980

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895490T= , CM000684.2:g.19895490T=	GRCh38
NC_000022.10:g.19883013T= , CM000684.1:g.19883013T=	GRCh37
NC_000022.9:g.18263013T=	NCBI36
NG_011835.1:g.51347A= , LRG_417:g.51347A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.866A= MANE Select	ENSP00000383365.1:p.Asp289=
ENST00000334363.14:c.866A=	ENSP00000334451.9:p.Asp289=
ENST00000400518.5:c.776A=	ENSP00000383362.1:p.Asp259=
ENST00000400519.6:c.863A=	ENSP00000383363.1:p.Asp288=
ENST00000400521.6:c.866A=	ENSP00000383365.1:p.Asp289=
ENST00000400525.6:c.797A=	ENSP00000383369.3:p.Asp266=
ENST00000474308.5:c.809A=	ENSP00000485665.1:p.Asp270=
ENST00000475995.3:c.363A=
ENST00000491939.6:c.770A=	ENSP00000485543.1:p.Asp257=
ENST00000494454.5:n.940A=
ENST00000542719.6:c.578A=	ENSP00000485128.2:p.Asp193=
ENST00000634537.1:c.95A=	ENSP00000489208.1:p.Asp32=
ENST00000635155.1:n.452A=
NM_001282512.1:c.866A=	NP_001269441.1:p.Asp289=
NM_006440.4:c.866A=	NP_006431.2:p.Asp289=
NM_001282512.2:c.866A=	NP_001269441.1:p.Asp289=
NM_001352300.1:c.863A=	NP_001339229.1:p.Asp288=
NM_001352301.1:c.776A=	NP_001339230.1:p.Asp259=
NM_001352302.1:c.578A=	NP_001339231.1:p.Asp193=
NM_001352303.1:c.770A=	NP_001339232.1:p.Asp257=
NR_147957.1:n.998A=
NM_006440.5:c.866A= MANE Select	NP_006431.2:p.Asp289=
NM_001282512.3:c.866A=	NP_001269441.1:p.Asp289=
NM_001352300.2:c.863A=	NP_001339229.1:p.Asp288=
NR_147957.2:n.824A=
NM_001352301.2:c.776A=	NP_001339230.1:p.Asp259=
NM_001352302.2:c.578A=	NP_001339231.1:p.Asp193=
NM_001352303.2:c.770A=	NP_001339232.1:p.Asp257=