Canonical Allele Identifier: CA410686788

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19895577-A-G
• MyVariant Identifiers: chr22:g.19883100A>G (hg19) ; chr22:g.19895577A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895577A>G , CM000684.2:g.19895577A>G	GRCh38
NC_000022.10:g.19883100A>G , CM000684.1:g.19883100A>G	GRCh37
NC_000022.9:g.18263100A>G	NCBI36
NG_011835.1:g.51260T>C , LRG_417:g.51260T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.779T>C MANE Select	ENSP00000383365.1:p.Met260Thr
ENST00000334363.14:c.779T>C	ENSP00000334451.9:p.Met260Thr
ENST00000400518.5:c.689T>C	ENSP00000383362.1:p.Met230Thr
ENST00000400519.6:c.776T>C	ENSP00000383363.1:p.Met259Thr
ENST00000400521.6:c.779T>C	ENSP00000383365.1:p.Met260Thr
ENST00000400525.6:c.710T>C	ENSP00000383369.3:p.Met237Thr
ENST00000474308.5:c.722T>C	ENSP00000485665.1:p.Met241Thr
ENST00000475995.3:c.276T>C
ENST00000491939.6:c.683T>C	ENSP00000485543.1:p.Met228Thr
ENST00000494454.5:n.853T>C
ENST00000542719.6:c.491T>C	ENSP00000485128.2:p.Met164Thr
ENST00000634537.1:c.8T>C	ENSP00000489208.1:p.Met3Thr
ENST00000635155.1:n.365T>C
NM_001282512.1:c.779T>C	NP_001269441.1:p.Met260Thr
NM_006440.4:c.779T>C	NP_006431.2:p.Met260Thr
NM_001282512.2:c.779T>C	NP_001269441.1:p.Met260Thr
NM_001352300.1:c.776T>C	NP_001339229.1:p.Met259Thr
NM_001352301.1:c.689T>C	NP_001339230.1:p.Met230Thr
NM_001352302.1:c.491T>C	NP_001339231.1:p.Met164Thr
NM_001352303.1:c.683T>C	NP_001339232.1:p.Met228Thr
NR_147957.1:n.911T>C
NM_006440.5:c.779T>C MANE Select	NP_006431.2:p.Met260Thr
NM_001282512.3:c.779T>C	NP_001269441.1:p.Met260Thr
NM_001352300.2:c.776T>C	NP_001339229.1:p.Met259Thr
NR_147957.2:n.737T>C
NM_001352301.2:c.689T>C	NP_001339230.1:p.Met230Thr
NM_001352302.2:c.491T>C	NP_001339231.1:p.Met164Thr
NM_001352303.2:c.683T>C	NP_001339232.1:p.Met228Thr