Canonical Allele Identifier: CA2988021378

Gene: TXNRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19880634dup , CM000684.2:g.19880634dup	GRCh38
NC_000022.10:g.19868157dup , CM000684.1:g.19868157dup	GRCh37
NC_000022.9:g.18248157dup	NCBI36
NG_011835.1:g.66204dup , LRG_417:g.66204dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.1171dup MANE Select	ENSP00000383365.1:p.Asp391GlyfsTer?
ENST00000400518.5:c.1081dup	ENSP00000383362.1:p.Asp361GlyfsTer?
ENST00000400519.6:c.1168dup	ENSP00000383363.1:p.Asp390GlyfsTer?
ENST00000400521.6:c.1171dup	ENSP00000383365.1:p.Asp391GlyfsTer?
ENST00000400525.6:c.1102dup	ENSP00000383369.3:p.Asp368GlyfsTer?
ENST00000462330.5:c.94dup	ENSP00000485603.2:p.Asp32GlyfsTer?
ENST00000462843.2:c.121dup	ENSP00000485466.2:p.Asp41GlyfsTer?
ENST00000474308.5:c.1114dup	ENSP00000485665.1:p.Asp372GlyfsTer?
ENST00000485358.5:c.139dup	ENSP00000485499.2:p.Asp47GlyfsTer?
ENST00000487165.5:n.1265dup
ENST00000494454.5:n.1245dup
ENST00000495655.2:n.715dup
ENST00000542719.6:c.883dup	ENSP00000485128.2:p.Asp295GlyfsTer?
ENST00000634471.1:n.244-362dup
ENST00000634537.1:c.400dup	ENSP00000489208.1:p.Asp134GlyfsTer?
NM_006440.4:c.1171dup	NP_006431.2:p.Asp391GlyfsTer?
NM_001352300.1:c.1168dup	NP_001339229.1:p.Asp390GlyfsTer?
NM_001352301.1:c.1081dup	NP_001339230.1:p.Asp361GlyfsTer?
NM_001352302.1:c.883dup	NP_001339231.1:p.Asp295GlyfsTer?
NR_147957.1:n.1303dup
NM_006440.5:c.1171dup MANE Select	NP_006431.2:p.Asp391GlyfsTer?
NM_001352300.2:c.1168dup	NP_001339229.1:p.Asp390GlyfsTer?
NR_147957.2:n.1129dup
NM_001352301.2:c.1081dup	NP_001339230.1:p.Asp361GlyfsTer?
NM_001352302.2:c.883dup	NP_001339231.1:p.Asp295GlyfsTer?