Canonical Allele Identifier: CA410682008

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868211G>C (hg19) ; chr22:g.19880688G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880688G>C , CM000684.2:g.19880688G>C	GRCh38
NC_000022.10:g.19868211G>C , CM000684.1:g.19868211G>C	GRCh37
NC_000022.9:g.18248211G>C	NCBI36
NG_011835.1:g.66149C>G , LRG_417:g.66149C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1116C>G MANE Select	ENSP00000383365.1:p.Ile372Met
ENST00000400518.5:c.1026C>G	ENSP00000383362.1:p.Ile342Met
ENST00000400519.6:c.1113C>G	ENSP00000383363.1:p.Ile371Met
ENST00000400521.6:c.1116C>G	ENSP00000383365.1:p.Ile372Met
ENST00000400525.6:c.1047C>G	ENSP00000383369.3:p.Ile349Met
ENST00000462330.5:c.39C>G	ENSP00000485603.2:p.Ile13Met
ENST00000462843.2:c.66C>G	ENSP00000485466.2:p.Ile22Met
ENST00000474308.5:c.1059C>G	ENSP00000485665.1:p.Ile353Met
ENST00000485358.5:c.84C>G	ENSP00000485499.2:p.Ile28Met
ENST00000487165.5:n.1210C>G
ENST00000494454.5:n.1190C>G
ENST00000495655.2:n.660C>G
ENST00000542719.6:c.828C>G	ENSP00000485128.2:p.Ile276Met
ENST00000634471.1:n.244-417C>G
ENST00000634537.1:c.345C>G	ENSP00000489208.1:p.Ile115Met
NM_006440.4:c.1116C>G	NP_006431.2:p.Ile372Met
NM_001352300.1:c.1113C>G	NP_001339229.1:p.Ile371Met
NM_001352301.1:c.1026C>G	NP_001339230.1:p.Ile342Met
NM_001352302.1:c.828C>G	NP_001339231.1:p.Ile276Met
NR_147957.1:n.1248C>G
NM_006440.5:c.1116C>G MANE Select	NP_006431.2:p.Ile372Met
NM_001352300.2:c.1113C>G	NP_001339229.1:p.Ile371Met
NR_147957.2:n.1074C>G
NM_001352301.2:c.1026C>G	NP_001339230.1:p.Ile342Met
NM_001352302.2:c.828C>G	NP_001339231.1:p.Ile276Met