Canonical Allele Identifier: CA410686629

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883022C>G (hg19) ; chr22:g.19895499C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895499C>G , CM000684.2:g.19895499C>G	GRCh38
NC_000022.10:g.19883022C>G , CM000684.1:g.19883022C>G	GRCh37
NC_000022.9:g.18263022C>G	NCBI36
NG_011835.1:g.51338G>C , LRG_417:g.51338G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.857G>C MANE Select	ENSP00000383365.1:p.Arg286Thr
ENST00000334363.14:c.857G>C	ENSP00000334451.9:p.Arg286Thr
ENST00000400518.5:c.767G>C	ENSP00000383362.1:p.Arg256Thr
ENST00000400519.6:c.854G>C	ENSP00000383363.1:p.Arg285Thr
ENST00000400521.6:c.857G>C	ENSP00000383365.1:p.Arg286Thr
ENST00000400525.6:c.788G>C	ENSP00000383369.3:p.Arg263Thr
ENST00000474308.5:c.800G>C	ENSP00000485665.1:p.Arg267Thr
ENST00000475995.3:c.354G>C
ENST00000491939.6:c.761G>C	ENSP00000485543.1:p.Arg254Thr
ENST00000494454.5:n.931G>C
ENST00000542719.6:c.569G>C	ENSP00000485128.2:p.Arg190Thr
ENST00000634537.1:c.86G>C	ENSP00000489208.1:p.Arg29Thr
ENST00000635155.1:n.443G>C
NM_001282512.1:c.857G>C	NP_001269441.1:p.Arg286Thr
NM_006440.4:c.857G>C	NP_006431.2:p.Arg286Thr
NM_001282512.2:c.857G>C	NP_001269441.1:p.Arg286Thr
NM_001352300.1:c.854G>C	NP_001339229.1:p.Arg285Thr
NM_001352301.1:c.767G>C	NP_001339230.1:p.Arg256Thr
NM_001352302.1:c.569G>C	NP_001339231.1:p.Arg190Thr
NM_001352303.1:c.761G>C	NP_001339232.1:p.Arg254Thr
NR_147957.1:n.989G>C
NM_006440.5:c.857G>C MANE Select	NP_006431.2:p.Arg286Thr
NM_001282512.3:c.857G>C	NP_001269441.1:p.Arg286Thr
NM_001352300.2:c.854G>C	NP_001339229.1:p.Arg285Thr
NR_147957.2:n.815G>C
NM_001352301.2:c.767G>C	NP_001339230.1:p.Arg256Thr
NM_001352302.2:c.569G>C	NP_001339231.1:p.Arg190Thr
NM_001352303.2:c.761G>C	NP_001339232.1:p.Arg254Thr