Canonical Allele Identifier: CA2396095243

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19902302G= , CM000684.2:g.19902302G=	GRCh38
NC_000022.10:g.19889825G= , CM000684.1:g.19889825G=	GRCh37
NC_000022.9:g.18269825G=	NCBI36
NG_011835.1:g.44535C= , LRG_417:g.44535C=

Transcript Alleles

HGVS	Amino-acid Change
NM_006440.5:c.663-3234C= MANE Select	NP_006431.2:n.663-3234C=
ENST00000400521.7:c.663-3234C= MANE Select	ENSP00000383365.1:n.663-3234C=
NM_001282512.1:c.663-3234C=	NP_001269441.1:n.663-3234C=
NM_001282512.2:c.663-3234C=	NP_001269441.1:n.663-3234C=
NM_001282512.3:c.663-3234C=	NP_001269441.1:n.663-3234C=
NM_001352300.1:c.660-3234C=	NP_001339229.1:n.660-3234C=
NM_001352300.2:c.660-3234C=	NP_001339229.1:n.660-3234C=
NM_001352301.1:c.573-3234C=	NP_001339230.1:n.573-3234C=
NM_001352301.2:c.573-3234C=	NP_001339230.1:n.573-3234C=
NM_001352302.1:c.375-3234C=	NP_001339231.1:n.375-3234C=
NM_001352302.2:c.375-3234C=	NP_001339231.1:n.375-3234C=
NM_001352303.1:c.567-3234C=	NP_001339232.1:n.567-3234C=
NM_001352303.2:c.567-3234C=	NP_001339232.1:n.567-3234C=
NM_006440.4:c.663-3234C=	NP_006431.2:n.663-3234C=
NR_147957.1:n.795-3234C=
NR_147957.2:n.621-3234C=
ENST00000334363.14:c.663-3234C=	ENSP00000334451.9:n.663-3234C=
ENST00000400518.5:c.573-3234C=	ENSP00000383362.1:n.573-3234C=
ENST00000400519.6:c.660-3234C=	ENSP00000383363.1:n.660-3234C=
ENST00000400521.6:c.663-3234C=	ENSP00000383365.1:n.663-3234C=
ENST00000400525.6:c.594-3234C=	ENSP00000383369.3:n.594-3234C=
ENST00000474308.5:c.606-3234C=	ENSP00000485665.1:n.606-3234C=
ENST00000475995.3:c.160-3234C=
ENST00000491939.6:c.567-3234C=	ENSP00000485543.1:n.567-3234C=
ENST00000494454.5:n.737-3234C=
ENST00000542719.6:c.375-3234C=	ENSP00000485128.2:n.375-3234C=
ENST00000635155.1:n.249-3234C=