Canonical Allele Identifier: CA410686569

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19895470-A-G
• MyVariant Identifiers: chr22:g.19882993A>G (hg19) ; chr22:g.19895470A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895470A>G , CM000684.2:g.19895470A>G	GRCh38
NC_000022.10:g.19882993A>G , CM000684.1:g.19882993A>G	GRCh37
NC_000022.9:g.18262993A>G	NCBI36
NG_011835.1:g.51367T>C , LRG_417:g.51367T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.886T>C MANE Select	ENSP00000383365.1:p.Trp296Arg
ENST00000334363.14:c.886T>C	ENSP00000334451.9:p.Trp296Arg
ENST00000400518.5:c.796T>C	ENSP00000383362.1:p.Trp266Arg
ENST00000400519.6:c.883T>C	ENSP00000383363.1:p.Trp295Arg
ENST00000400521.6:c.886T>C	ENSP00000383365.1:p.Trp296Arg
ENST00000400525.6:c.817T>C	ENSP00000383369.3:p.Trp273Arg
ENST00000474308.5:c.829T>C	ENSP00000485665.1:p.Trp277Arg
ENST00000475995.3:c.383T>C
ENST00000491939.6:c.790T>C	ENSP00000485543.1:p.Trp264Arg
ENST00000494454.5:n.960T>C
ENST00000542719.6:c.598T>C	ENSP00000485128.2:p.Trp200Arg
ENST00000634537.1:c.115T>C	ENSP00000489208.1:p.Trp39Arg
ENST00000635155.1:n.472T>C
NM_001282512.1:c.886T>C	NP_001269441.1:p.Trp296Arg
NM_006440.4:c.886T>C	NP_006431.2:p.Trp296Arg
NM_001282512.2:c.886T>C	NP_001269441.1:p.Trp296Arg
NM_001352300.1:c.883T>C	NP_001339229.1:p.Trp295Arg
NM_001352301.1:c.796T>C	NP_001339230.1:p.Trp266Arg
NM_001352302.1:c.598T>C	NP_001339231.1:p.Trp200Arg
NM_001352303.1:c.790T>C	NP_001339232.1:p.Trp264Arg
NR_147957.1:n.1018T>C
NM_006440.5:c.886T>C MANE Select	NP_006431.2:p.Trp296Arg
NM_001282512.3:c.886T>C	NP_001269441.1:p.Trp296Arg
NM_001352300.2:c.883T>C	NP_001339229.1:p.Trp295Arg
NR_147957.2:n.844T>C
NM_001352301.2:c.796T>C	NP_001339230.1:p.Trp266Arg
NM_001352302.2:c.598T>C	NP_001339231.1:p.Trp200Arg
NM_001352303.2:c.790T>C	NP_001339232.1:p.Trp264Arg