Canonical Allele Identifier: CA2396114840
Gene: TXNRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1941697495

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19941122_19941128dup , CM000684.2:g.19941122_19941128dup GRCh38
NC_000022.10:g.19928645_19928651dup , CM000684.1:g.19928645_19928651dup GRCh37
NC_000022.9:g.18308645_18308651dup NCBI36
NG_011526.1:g.4383_4389dup
NG_011835.1:g.5712_5718dup , LRG_417:g.5712_5718dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000400521.7:c.103+576_103+582dup MANE Select ENSP00000383365.1:n.103+576_103+582dup
ENST00000334363.14:c.103+576_103+582dup ENSP00000334451.9:n.103+576_103+582dup
ENST00000400519.6:c.103+576_103+582dup ENSP00000383363.1:n.103+576_103+582dup
ENST00000400521.6:c.103+576_103+582dup ENSP00000383365.1:n.103+576_103+582dup
ENST00000400525.6:c.103+576_103+582dup ENSP00000383369.3:n.103+576_103+582dup
ENST00000474308.5:c.103+576_103+582dup ENSP00000485665.1:n.103+576_103+582dup
ENST00000496729.2:n.108+576_108+582dup
NM_001282512.1:c.103+576_103+582dup NP_001269441.1:n.103+576_103+582dup
NM_006440.4:c.103+576_103+582dup NP_006431.2:n.103+576_103+582dup
NM_001282512.2:c.103+576_103+582dup NP_001269441.1:n.103+576_103+582dup
NM_001352300.1:c.103+576_103+582dup NP_001339229.1:n.103+576_103+582dup
NR_147957.1:n.292+576_292+582dup
NM_006440.5:c.103+576_103+582dup MANE Select NP_006431.2:n.103+576_103+582dup
NM_001282512.3:c.103+576_103+582dup NP_001269441.1:n.103+576_103+582dup
NM_001352300.2:c.103+576_103+582dup NP_001339229.1:n.103+576_103+582dup
NR_147957.2:n.118+576_118+582dup