Canonical Allele Identifier: CA410682012

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868213T>C (hg19) ; chr22:g.19880690T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880690T>C , CM000684.2:g.19880690T>C	GRCh38
NC_000022.10:g.19868213T>C , CM000684.1:g.19868213T>C	GRCh37
NC_000022.9:g.18248213T>C	NCBI36
NG_011835.1:g.66147A>G , LRG_417:g.66147A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1114A>G MANE Select	ENSP00000383365.1:p.Ile372Val
ENST00000400518.5:c.1024A>G	ENSP00000383362.1:p.Ile342Val
ENST00000400519.6:c.1111A>G	ENSP00000383363.1:p.Ile371Val
ENST00000400521.6:c.1114A>G	ENSP00000383365.1:p.Ile372Val
ENST00000400525.6:c.1045A>G	ENSP00000383369.3:p.Ile349Val
ENST00000462330.5:c.37A>G	ENSP00000485603.2:p.Ile13Val
ENST00000462843.2:c.64A>G	ENSP00000485466.2:p.Ile22Val
ENST00000474308.5:c.1057A>G	ENSP00000485665.1:p.Ile353Val
ENST00000485358.5:c.82A>G	ENSP00000485499.2:p.Ile28Val
ENST00000487165.5:n.1208A>G
ENST00000494454.5:n.1188A>G
ENST00000495655.2:n.658A>G
ENST00000542719.6:c.826A>G	ENSP00000485128.2:p.Ile276Val
ENST00000634471.1:n.244-419A>G
ENST00000634537.1:c.343A>G	ENSP00000489208.1:p.Ile115Val
NM_006440.4:c.1114A>G	NP_006431.2:p.Ile372Val
NM_001352300.1:c.1111A>G	NP_001339229.1:p.Ile371Val
NM_001352301.1:c.1024A>G	NP_001339230.1:p.Ile342Val
NM_001352302.1:c.826A>G	NP_001339231.1:p.Ile276Val
NR_147957.1:n.1246A>G
NM_006440.5:c.1114A>G MANE Select	NP_006431.2:p.Ile372Val
NM_001352300.2:c.1111A>G	NP_001339229.1:p.Ile371Val
NR_147957.2:n.1072A>G
NM_001352301.2:c.1024A>G	NP_001339230.1:p.Ile342Val
NM_001352302.2:c.826A>G	NP_001339231.1:p.Ile276Val