Canonical Allele Identifier: CA2396092013

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895569T= , CM000684.2:g.19895569T=	GRCh38
NC_000022.10:g.19883092T= , CM000684.1:g.19883092T=	GRCh37
NC_000022.9:g.18263092T=	NCBI36
NG_011835.1:g.51268A= , LRG_417:g.51268A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.787A= MANE Select	ENSP00000383365.1:p.Met263=
ENST00000334363.14:c.787A=	ENSP00000334451.9:p.Met263=
ENST00000400518.5:c.697A=	ENSP00000383362.1:p.Met233=
ENST00000400519.6:c.784A=	ENSP00000383363.1:p.Met262=
ENST00000400521.6:c.787A=	ENSP00000383365.1:p.Met263=
ENST00000400525.6:c.718A=	ENSP00000383369.3:p.Met240=
ENST00000474308.5:c.730A=	ENSP00000485665.1:p.Met244=
ENST00000475995.3:c.284A=
ENST00000491939.6:c.691A=	ENSP00000485543.1:p.Met231=
ENST00000494454.5:n.861A=
ENST00000542719.6:c.499A=	ENSP00000485128.2:p.Met167=
ENST00000634537.1:c.16A=	ENSP00000489208.1:p.Met6=
ENST00000635155.1:n.373A=
NM_001282512.1:c.787A=	NP_001269441.1:p.Met263=
NM_006440.4:c.787A=	NP_006431.2:p.Met263=
NM_001282512.2:c.787A=	NP_001269441.1:p.Met263=
NM_001352300.1:c.784A=	NP_001339229.1:p.Met262=
NM_001352301.1:c.697A=	NP_001339230.1:p.Met233=
NM_001352302.1:c.499A=	NP_001339231.1:p.Met167=
NM_001352303.1:c.691A=	NP_001339232.1:p.Met231=
NR_147957.1:n.919A=
NM_006440.5:c.787A= MANE Select	NP_006431.2:p.Met263=
NM_001282512.3:c.787A=	NP_001269441.1:p.Met263=
NM_001352300.2:c.784A=	NP_001339229.1:p.Met262=
NR_147957.2:n.745A=
NM_001352301.2:c.697A=	NP_001339230.1:p.Met233=
NM_001352302.2:c.499A=	NP_001339231.1:p.Met167=
NM_001352303.2:c.691A=	NP_001339232.1:p.Met231=