Canonical Allele Identifier: CA410686756

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19895563-T-C
• MyVariant Identifiers: chr22:g.19883086T>C (hg19) ; chr22:g.19895563T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895563T>C , CM000684.2:g.19895563T>C	GRCh38
NC_000022.10:g.19883086T>C , CM000684.1:g.19883086T>C	GRCh37
NC_000022.9:g.18263086T>C	NCBI36
NG_011835.1:g.51274A>G , LRG_417:g.51274A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.793A>G MANE Select	ENSP00000383365.1:p.Ile265Val
ENST00000334363.14:c.793A>G	ENSP00000334451.9:p.Ile265Val
ENST00000400518.5:c.703A>G	ENSP00000383362.1:p.Ile235Val
ENST00000400519.6:c.790A>G	ENSP00000383363.1:p.Ile264Val
ENST00000400521.6:c.793A>G	ENSP00000383365.1:p.Ile265Val
ENST00000400525.6:c.724A>G	ENSP00000383369.3:p.Ile242Val
ENST00000474308.5:c.736A>G	ENSP00000485665.1:p.Ile246Val
ENST00000475995.3:c.290A>G
ENST00000491939.6:c.697A>G	ENSP00000485543.1:p.Ile233Val
ENST00000494454.5:n.867A>G
ENST00000542719.6:c.505A>G	ENSP00000485128.2:p.Ile169Val
ENST00000634537.1:c.22A>G	ENSP00000489208.1:p.Ile8Val
ENST00000635155.1:n.379A>G
NM_001282512.1:c.793A>G	NP_001269441.1:p.Ile265Val
NM_006440.4:c.793A>G	NP_006431.2:p.Ile265Val
NM_001282512.2:c.793A>G	NP_001269441.1:p.Ile265Val
NM_001352300.1:c.790A>G	NP_001339229.1:p.Ile264Val
NM_001352301.1:c.703A>G	NP_001339230.1:p.Ile235Val
NM_001352302.1:c.505A>G	NP_001339231.1:p.Ile169Val
NM_001352303.1:c.697A>G	NP_001339232.1:p.Ile233Val
NR_147957.1:n.925A>G
NM_006440.5:c.793A>G MANE Select	NP_006431.2:p.Ile265Val
NM_001282512.3:c.793A>G	NP_001269441.1:p.Ile265Val
NM_001352300.2:c.790A>G	NP_001339229.1:p.Ile264Val
NR_147957.2:n.751A>G
NM_001352301.2:c.703A>G	NP_001339230.1:p.Ile235Val
NM_001352302.2:c.505A>G	NP_001339231.1:p.Ile169Val
NM_001352303.2:c.697A>G	NP_001339232.1:p.Ile233Val