Canonical Allele Identifier: CA410681937

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19868173C>T (hg19) ; chr22:g.19880650C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880650C>T , CM000684.2:g.19880650C>T	GRCh38
NC_000022.10:g.19868173C>T , CM000684.1:g.19868173C>T	GRCh37
NC_000022.9:g.18248173C>T	NCBI36
NG_011835.1:g.66187G>A , LRG_417:g.66187G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1154G>A MANE Select	ENSP00000383365.1:p.Gly385Glu
ENST00000400518.5:c.1064G>A	ENSP00000383362.1:p.Gly355Glu
ENST00000400519.6:c.1151G>A	ENSP00000383363.1:p.Gly384Glu
ENST00000400521.6:c.1154G>A	ENSP00000383365.1:p.Gly385Glu
ENST00000400525.6:c.1085G>A	ENSP00000383369.3:p.Gly362Glu
ENST00000462330.5:c.77G>A	ENSP00000485603.2:p.Gly26Glu
ENST00000462843.2:c.104G>A	ENSP00000485466.2:p.Gly35Glu
ENST00000474308.5:c.1097G>A	ENSP00000485665.1:p.Gly366Glu
ENST00000485358.5:c.122G>A	ENSP00000485499.2:p.Gly41Glu
ENST00000487165.5:n.1248G>A
ENST00000494454.5:n.1228G>A
ENST00000495655.2:n.698G>A
ENST00000542719.6:c.866G>A	ENSP00000485128.2:p.Gly289Glu
ENST00000634471.1:n.244-379G>A
ENST00000634537.1:c.383G>A	ENSP00000489208.1:p.Gly128Glu
NM_006440.4:c.1154G>A	NP_006431.2:p.Gly385Glu
NM_001352300.1:c.1151G>A	NP_001339229.1:p.Gly384Glu
NM_001352301.1:c.1064G>A	NP_001339230.1:p.Gly355Glu
NM_001352302.1:c.866G>A	NP_001339231.1:p.Gly289Glu
NR_147957.1:n.1286G>A
NM_006440.5:c.1154G>A MANE Select	NP_006431.2:p.Gly385Glu
NM_001352300.2:c.1151G>A	NP_001339229.1:p.Gly384Glu
NR_147957.2:n.1112G>A
NM_001352301.2:c.1064G>A	NP_001339230.1:p.Gly355Glu
NM_001352302.2:c.866G>A	NP_001339231.1:p.Gly289Glu