Canonical Allele Identifier: CA10103703

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19878405G>A , CM000684.2:g.19878405G>A	GRCh38
NC_000022.10:g.19865928G>A , CM000684.1:g.19865928G>A	GRCh37
NC_000022.9:g.18245928G>A	NCBI36
NG_011835.1:g.68432C>T , LRG_417:g.68432C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006440.5:c.1308C>T MANE Select	NP_006431.2:p.Phe436=
ENST00000400521.7:c.1308C>T MANE Select	ENSP00000383365.1:p.Phe436=
NM_001352300.1:c.1305C>T	NP_001339229.1:p.Phe435=
NM_001352300.2:c.1305C>T	NP_001339229.1:p.Phe435=
NM_001352301.1:c.1218C>T	NP_001339230.1:p.Phe406=
NM_001352301.2:c.1218C>T	NP_001339230.1:p.Phe406=
NM_001352302.1:c.1020C>T	NP_001339231.1:p.Phe340=
NM_001352302.2:c.1020C>T	NP_001339231.1:p.Phe340=
NM_006440.4:c.1308C>T	NP_006431.2:p.Phe436=
NR_147957.1:n.1440C>T
NR_147957.2:n.1266C>T
ENST00000400518.5:c.1218C>T	ENSP00000383362.1:p.Phe406=
ENST00000400519.6:c.1305C>T	ENSP00000383363.1:p.Phe435=
ENST00000400521.6:c.1308C>T	ENSP00000383365.1:p.Phe436=
ENST00000400525.6:c.1239C>T	ENSP00000383369.3:p.Phe413=
ENST00000462330.5:c.231C>T	ENSP00000485603.2:p.Phe77=
ENST00000462843.2:c.258C>T	ENSP00000485466.2:p.Phe86=
ENST00000474308.5:c.1251C>T	ENSP00000485665.1:p.Phe417=
ENST00000485358.5:c.276C>T	ENSP00000485499.2:p.Phe92=
ENST00000487165.5:n.1402C>T
ENST00000494454.5:n.1382C>T
ENST00000495655.2:n.852C>T
ENST00000542719.6:c.1020C>T	ENSP00000485128.2:p.Phe340=
ENST00000634471.1:n.369C>T
ENST00000634537.1:c.537C>T	ENSP00000489208.1:p.Phe179=