Canonical Allele Identifier: CA410686751

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883084T>C (hg19) ; chr22:g.19895561T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895561T>C , CM000684.2:g.19895561T>C	GRCh38
NC_000022.10:g.19883084T>C , CM000684.1:g.19883084T>C	GRCh37
NC_000022.9:g.18263084T>C	NCBI36
NG_011835.1:g.51276A>G , LRG_417:g.51276A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.795A>G MANE Select	ENSP00000383365.1:p.Ile265Met
ENST00000334363.14:c.795A>G	ENSP00000334451.9:p.Ile265Met
ENST00000400518.5:c.705A>G	ENSP00000383362.1:p.Ile235Met
ENST00000400519.6:c.792A>G	ENSP00000383363.1:p.Ile264Met
ENST00000400521.6:c.795A>G	ENSP00000383365.1:p.Ile265Met
ENST00000400525.6:c.726A>G	ENSP00000383369.3:p.Ile242Met
ENST00000474308.5:c.738A>G	ENSP00000485665.1:p.Ile246Met
ENST00000475995.3:c.292A>G
ENST00000491939.6:c.699A>G	ENSP00000485543.1:p.Ile233Met
ENST00000494454.5:n.869A>G
ENST00000542719.6:c.507A>G	ENSP00000485128.2:p.Ile169Met
ENST00000634537.1:c.24A>G	ENSP00000489208.1:p.Ile8Met
ENST00000635155.1:n.381A>G
NM_001282512.1:c.795A>G	NP_001269441.1:p.Ile265Met
NM_006440.4:c.795A>G	NP_006431.2:p.Ile265Met
NM_001282512.2:c.795A>G	NP_001269441.1:p.Ile265Met
NM_001352300.1:c.792A>G	NP_001339229.1:p.Ile264Met
NM_001352301.1:c.705A>G	NP_001339230.1:p.Ile235Met
NM_001352302.1:c.507A>G	NP_001339231.1:p.Ile169Met
NM_001352303.1:c.699A>G	NP_001339232.1:p.Ile233Met
NR_147957.1:n.927A>G
NM_006440.5:c.795A>G MANE Select	NP_006431.2:p.Ile265Met
NM_001282512.3:c.795A>G	NP_001269441.1:p.Ile265Met
NM_001352300.2:c.792A>G	NP_001339229.1:p.Ile264Met
NR_147957.2:n.753A>G
NM_001352301.2:c.705A>G	NP_001339230.1:p.Ile235Met
NM_001352302.2:c.507A>G	NP_001339231.1:p.Ile169Met
NM_001352303.2:c.699A>G	NP_001339232.1:p.Ile233Met