Canonical Allele Identifier: CA410686639

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19895503-T-C
• MyVariant Identifiers: chr22:g.19883026T>C (hg19) ; chr22:g.19895503T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895503T>C , CM000684.2:g.19895503T>C	GRCh38
NC_000022.10:g.19883026T>C , CM000684.1:g.19883026T>C	GRCh37
NC_000022.9:g.18263026T>C	NCBI36
NG_011835.1:g.51334A>G , LRG_417:g.51334A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.853A>G MANE Select	ENSP00000383365.1:p.Arg285Gly
ENST00000334363.14:c.853A>G	ENSP00000334451.9:p.Arg285Gly
ENST00000400518.5:c.763A>G	ENSP00000383362.1:p.Arg255Gly
ENST00000400519.6:c.850A>G	ENSP00000383363.1:p.Arg284Gly
ENST00000400521.6:c.853A>G	ENSP00000383365.1:p.Arg285Gly
ENST00000400525.6:c.784A>G	ENSP00000383369.3:p.Arg262Gly
ENST00000474308.5:c.796A>G	ENSP00000485665.1:p.Arg266Gly
ENST00000475995.3:c.350A>G
ENST00000491939.6:c.757A>G	ENSP00000485543.1:p.Arg253Gly
ENST00000494454.5:n.927A>G
ENST00000542719.6:c.565A>G	ENSP00000485128.2:p.Arg189Gly
ENST00000634537.1:c.82A>G	ENSP00000489208.1:p.Arg28Gly
ENST00000635155.1:n.439A>G
NM_001282512.1:c.853A>G	NP_001269441.1:p.Arg285Gly
NM_006440.4:c.853A>G	NP_006431.2:p.Arg285Gly
NM_001282512.2:c.853A>G	NP_001269441.1:p.Arg285Gly
NM_001352300.1:c.850A>G	NP_001339229.1:p.Arg284Gly
NM_001352301.1:c.763A>G	NP_001339230.1:p.Arg255Gly
NM_001352302.1:c.565A>G	NP_001339231.1:p.Arg189Gly
NM_001352303.1:c.757A>G	NP_001339232.1:p.Arg253Gly
NR_147957.1:n.985A>G
NM_006440.5:c.853A>G MANE Select	NP_006431.2:p.Arg285Gly
NM_001282512.3:c.853A>G	NP_001269441.1:p.Arg285Gly
NM_001352300.2:c.850A>G	NP_001339229.1:p.Arg284Gly
NR_147957.2:n.811A>G
NM_001352301.2:c.763A>G	NP_001339230.1:p.Arg255Gly
NM_001352302.2:c.565A>G	NP_001339231.1:p.Arg189Gly
NM_001352303.2:c.757A>G	NP_001339232.1:p.Arg253Gly