Canonical Allele Identifier: CA410686268

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19882930C>G (hg19) ; chr22:g.19895407C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895407C>G , CM000684.2:g.19895407C>G	GRCh38
NC_000022.10:g.19882930C>G , CM000684.1:g.19882930C>G	GRCh37
NC_000022.9:g.18262930C>G	NCBI36
NG_011835.1:g.51430G>C , LRG_417:g.51430G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.949G>C MANE Select	ENSP00000383365.1:p.Gly317Arg
ENST00000334363.14:c.949G>C	ENSP00000334451.9:p.Ala317Pro
ENST00000400518.5:c.859G>C	ENSP00000383362.1:p.Gly287Arg
ENST00000400519.6:c.946G>C	ENSP00000383363.1:p.Gly316Arg
ENST00000400521.6:c.949G>C	ENSP00000383365.1:p.Gly317Arg
ENST00000400525.6:c.880G>C	ENSP00000383369.3:p.Gly294Arg
ENST00000474308.5:c.892G>C	ENSP00000485665.1:p.Gly298Arg
ENST00000475995.3:c.446G>C
ENST00000491939.6:c.853G>C	ENSP00000485543.1:p.Ala285Pro
ENST00000494454.5:n.1023G>C
ENST00000542719.6:c.661G>C	ENSP00000485128.2:p.Gly221Arg
ENST00000634537.1:c.178G>C	ENSP00000489208.1:p.Gly60Arg
ENST00000635155.1:n.535G>C
NM_001282512.1:c.949G>C	NP_001269441.1:p.Ala317Pro
NM_006440.4:c.949G>C	NP_006431.2:p.Gly317Arg
NM_001282512.2:c.949G>C	NP_001269441.1:p.Ala317Pro
NM_001352300.1:c.946G>C	NP_001339229.1:p.Gly316Arg
NM_001352301.1:c.859G>C	NP_001339230.1:p.Gly287Arg
NM_001352302.1:c.661G>C	NP_001339231.1:p.Gly221Arg
NM_001352303.1:c.853G>C	NP_001339232.1:p.Ala285Pro
NR_147957.1:n.1081G>C
NM_006440.5:c.949G>C MANE Select	NP_006431.2:p.Gly317Arg
NM_001282512.3:c.949G>C	NP_001269441.1:p.Ala317Pro
NM_001352300.2:c.946G>C	NP_001339229.1:p.Gly316Arg
NR_147957.2:n.907G>C
NM_001352301.2:c.859G>C	NP_001339230.1:p.Gly287Arg
NM_001352302.2:c.661G>C	NP_001339231.1:p.Gly221Arg
NM_001352303.2:c.853G>C	NP_001339232.1:p.Ala285Pro