Canonical Allele Identifier: CA410694028

Gene: TXNRD2

Linked Data

• gnomAD v4: 22-19918978-A-G
• COSMIC: COSM5447446 ; COSM5447447
• MyVariant Identifiers: chr22:g.19906501A>G (hg19) ; chr22:g.19918978A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19918978A>G , CM000684.2:g.19918978A>G	GRCh38
NC_000022.10:g.19906501A>G , CM000684.1:g.19906501A>G	GRCh37
NC_000022.9:g.18286501A>G	NCBI36
NG_011835.1:g.27859T>C , LRG_417:g.27859T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.256T>C MANE Select	ENSP00000383365.1:p.Cys86Arg
ENST00000334363.14:c.256T>C	ENSP00000334451.9:p.Cys86Arg
ENST00000400518.5:c.166T>C	ENSP00000383362.1:p.Cys56Arg
ENST00000400519.6:c.253T>C	ENSP00000383363.1:p.Cys85Arg
ENST00000400521.6:c.256T>C	ENSP00000383365.1:p.Cys86Arg
ENST00000400525.6:c.187T>C	ENSP00000383369.3:p.Cys63Arg
ENST00000474308.5:c.199T>C	ENSP00000485665.1:p.Cys67Arg
ENST00000491939.6:c.160T>C	ENSP00000485543.1:p.Cys54Arg
ENST00000496729.2:n.261T>C
ENST00000542719.6:c.-33T>C	ENSP00000485128.2:n.-33T>C
NM_001282512.1:c.256T>C	NP_001269441.1:p.Cys86Arg
NM_006440.4:c.256T>C	NP_006431.2:p.Cys86Arg
NM_001282512.2:c.256T>C	NP_001269441.1:p.Cys86Arg
NM_001352300.1:c.253T>C	NP_001339229.1:p.Cys85Arg
NM_001352301.1:c.166T>C	NP_001339230.1:p.Cys56Arg
NM_001352302.1:c.-33T>C	NP_001339231.1:n.-33T>C
NM_001352303.1:c.160T>C	NP_001339232.1:p.Cys54Arg
NR_147957.1:n.388T>C
NM_006440.5:c.256T>C MANE Select	NP_006431.2:p.Cys86Arg
NM_001282512.3:c.256T>C	NP_001269441.1:p.Cys86Arg
NM_001352300.2:c.253T>C	NP_001339229.1:p.Cys85Arg
NR_147957.2:n.214T>C
NM_001352301.2:c.166T>C	NP_001339230.1:p.Cys56Arg
NM_001352302.2:c.-33T>C	NP_001339231.1:n.-33T>C
NM_001352303.2:c.160T>C	NP_001339232.1:p.Cys54Arg