Canonical Allele Identifier: CA10103743

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880259C>T , CM000684.2:g.19880259C>T	GRCh38
NC_000022.10:g.19867782C>T , CM000684.1:g.19867782C>T	GRCh37
NC_000022.9:g.18247782C>T	NCBI36
NG_011835.1:g.66578G>A , LRG_417:g.66578G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1195G>A MANE Select	ENSP00000383365.1:p.Val399Ile
ENST00000400518.5:c.1105G>A	ENSP00000383362.1:p.Val369Ile
ENST00000400519.6:c.1192G>A	ENSP00000383363.1:p.Val398Ile
ENST00000400521.6:c.1195G>A	ENSP00000383365.1:p.Val399Ile
ENST00000400525.6:c.1126G>A	ENSP00000383369.3:p.Val376Ile
ENST00000462330.5:c.118G>A	ENSP00000485603.2:p.Val40Ile
ENST00000462843.2:c.145G>A	ENSP00000485466.2:p.Val49Ile
ENST00000474308.5:c.1138G>A	ENSP00000485665.1:p.Val380Ile
ENST00000485358.5:c.163G>A	ENSP00000485499.2:p.Val55Ile
ENST00000487165.5:n.1289G>A
ENST00000494454.5:n.1269G>A
ENST00000495655.2:n.739G>A
ENST00000542719.6:c.907G>A	ENSP00000485128.2:p.Val303Ile
ENST00000634471.1:n.256G>A
ENST00000634537.1:c.424G>A	ENSP00000489208.1:p.Val142Ile
NM_006440.4:c.1195G>A	NP_006431.2:p.Val399Ile
NM_001352300.1:c.1192G>A	NP_001339229.1:p.Val398Ile
NM_001352301.1:c.1105G>A	NP_001339230.1:p.Val369Ile
NM_001352302.1:c.907G>A	NP_001339231.1:p.Val303Ile
NR_147957.1:n.1327G>A
NM_006440.5:c.1195G>A MANE Select	NP_006431.2:p.Val399Ile
NM_001352300.2:c.1192G>A	NP_001339229.1:p.Val398Ile
NR_147957.2:n.1153G>A
NM_001352301.2:c.1105G>A	NP_001339230.1:p.Val369Ile
NM_001352302.2:c.907G>A	NP_001339231.1:p.Val303Ile