Canonical Allele Identifier: CA513365282

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883030C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895507C>G , CM000684.2:g.19895507C>G	GRCh38
NC_000022.10:g.19883030C>G , CM000684.1:g.19883030C>G	GRCh37
NC_000022.9:g.18263030C>G	NCBI36
NG_011835.1:g.51330G>C , LRG_417:g.51330G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.849G>C MANE Select	ENSP00000383365.1:p.Arg283=
ENST00000334363.14:c.849G>C	ENSP00000334451.9:p.Arg283=
ENST00000400518.5:c.759G>C	ENSP00000383362.1:p.Arg253=
ENST00000400519.6:c.846G>C	ENSP00000383363.1:p.Arg282=
ENST00000400521.6:c.849G>C	ENSP00000383365.1:p.Arg283=
ENST00000400525.6:c.780G>C	ENSP00000383369.3:p.Arg260=
ENST00000474308.5:c.792G>C	ENSP00000485665.1:p.Arg264=
ENST00000475995.3:c.346G>C
ENST00000491939.6:c.753G>C	ENSP00000485543.1:p.Arg251=
ENST00000494454.5:n.923G>C
ENST00000542719.6:c.561G>C	ENSP00000485128.2:p.Arg187=
ENST00000634537.1:c.78G>C	ENSP00000489208.1:p.Arg26=
ENST00000635155.1:n.435G>C
NM_001282512.1:c.849G>C	NP_001269441.1:p.Arg283=
NM_006440.4:c.849G>C	NP_006431.2:p.Arg283=
NM_001282512.2:c.849G>C	NP_001269441.1:p.Arg283=
NM_001352300.1:c.846G>C	NP_001339229.1:p.Arg282=
NM_001352301.1:c.759G>C	NP_001339230.1:p.Arg253=
NM_001352302.1:c.561G>C	NP_001339231.1:p.Arg187=
NM_001352303.1:c.753G>C	NP_001339232.1:p.Arg251=
NR_147957.1:n.981G>C
NM_006440.5:c.849G>C MANE Select	NP_006431.2:p.Arg283=
NM_001282512.3:c.849G>C	NP_001269441.1:p.Arg283=
NM_001352300.2:c.846G>C	NP_001339229.1:p.Arg282=
NR_147957.2:n.807G>C
NM_001352301.2:c.759G>C	NP_001339230.1:p.Arg253=
NM_001352302.2:c.561G>C	NP_001339231.1:p.Arg187=
NM_001352303.2:c.753G>C	NP_001339232.1:p.Arg251=