Canonical Allele Identifier: CA751471597

Gene: TXNRD2

Linked Data

• dbSNP Id: rs1226122710
• gnomAD v3: 22-19941147-A-ATC
• gnomAD v4: 22-19941147-A-ATC
• MyVariant Identifiers: chr22:g.19928670_19928671insTC (hg19) ; chr22:g.19941147_19941148insTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19941149_19941150dup , CM000684.2:g.19941149_19941150dup	GRCh38
NC_000022.10:g.19928672_19928673dup , CM000684.1:g.19928672_19928673dup	GRCh37
NC_000022.9:g.18308672_18308673dup	NCBI36
NG_011526.1:g.4410_4411dup
NG_011835.1:g.5688_5689dup , LRG_417:g.5688_5689dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000400521.7:c.103+552_103+553dup MANE Select	ENSP00000383365.1:n.103+552_103+553dup
ENST00000334363.14:c.103+552_103+553dup	ENSP00000334451.9:n.103+552_103+553dup
ENST00000400519.6:c.103+552_103+553dup	ENSP00000383363.1:n.103+552_103+553dup
ENST00000400521.6:c.103+552_103+553dup	ENSP00000383365.1:n.103+552_103+553dup
ENST00000400525.6:c.103+552_103+553dup	ENSP00000383369.3:n.103+552_103+553dup
ENST00000474308.5:c.103+552_103+553dup	ENSP00000485665.1:n.103+552_103+553dup
ENST00000496729.2:n.108+552_108+553dup
NM_001282512.1:c.103+552_103+553dup	NP_001269441.1:n.103+552_103+553dup
NM_006440.4:c.103+552_103+553dup	NP_006431.2:n.103+552_103+553dup
NM_001282512.2:c.103+552_103+553dup	NP_001269441.1:n.103+552_103+553dup
NM_001352300.1:c.103+552_103+553dup	NP_001339229.1:n.103+552_103+553dup
NR_147957.1:n.292+552_292+553dup
NM_006440.5:c.103+552_103+553dup MANE Select	NP_006431.2:n.103+552_103+553dup
NM_001282512.3:c.103+552_103+553dup	NP_001269441.1:n.103+552_103+553dup
NM_001352300.2:c.103+552_103+553dup	NP_001339229.1:n.103+552_103+553dup
NR_147957.2:n.118+552_118+553dup