Canonical Allele Identifier: CA2396103797

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918992C= , CM000684.2:g.19918992C=	GRCh38
NC_000022.10:g.19906515C= , CM000684.1:g.19906515C=	GRCh37
NC_000022.9:g.18286515C=	NCBI36
NG_011835.1:g.27845G= , LRG_417:g.27845G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.242G= MANE Select	ENSP00000383365.1:p.Gly81=
ENST00000334363.14:c.242G=	ENSP00000334451.9:p.Gly81=
ENST00000400518.5:c.152G=	ENSP00000383362.1:p.Gly51=
ENST00000400519.6:c.239G=	ENSP00000383363.1:p.Gly80=
ENST00000400521.6:c.242G=	ENSP00000383365.1:p.Gly81=
ENST00000400525.6:c.173G=	ENSP00000383369.3:p.Gly58=
ENST00000474308.5:c.185G=	ENSP00000485665.1:p.Gly62=
ENST00000491939.6:c.146G=	ENSP00000485543.1:p.Gly49=
ENST00000496729.2:n.247G=
ENST00000542719.6:c.-47G=	ENSP00000485128.2:n.-47G=
NM_001282512.1:c.242G=	NP_001269441.1:p.Gly81=
NM_006440.4:c.242G=	NP_006431.2:p.Gly81=
NM_001282512.2:c.242G=	NP_001269441.1:p.Gly81=
NM_001352300.1:c.239G=	NP_001339229.1:p.Gly80=
NM_001352301.1:c.152G=	NP_001339230.1:p.Gly51=
NM_001352302.1:c.-47G=	NP_001339231.1:n.-47G=
NM_001352303.1:c.146G=	NP_001339232.1:p.Gly49=
NR_147957.1:n.374G=
NM_006440.5:c.242G= MANE Select	NP_006431.2:p.Gly81=
NM_001282512.3:c.242G=	NP_001269441.1:p.Gly81=
NM_001352300.2:c.239G=	NP_001339229.1:p.Gly80=
NR_147957.2:n.200G=
NM_001352301.2:c.152G=	NP_001339230.1:p.Gly51=
NM_001352302.2:c.-47G=	NP_001339231.1:n.-47G=
NM_001352303.2:c.146G=	NP_001339232.1:p.Gly49=