Canonical Allele Identifier: CA1024161157
Gene: TXNRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1941699556

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19941186_19941190del , CM000684.2:g.19941186_19941190del GRCh38
NC_000022.10:g.19928709_19928713del , CM000684.1:g.19928709_19928713del GRCh37
NC_000022.9:g.18308709_18308713del NCBI36
NG_011526.1:g.4447_4451del
NG_011835.1:g.5650_5654del , LRG_417:g.5650_5654del

Transcript Alleles

HGVS Amino-acid change
ENST00000400521.7:c.103+514_103+518del MANE Select ENSP00000383365.1:n.103+514_103+518del
ENST00000334363.14:c.103+514_103+518del ENSP00000334451.9:n.103+514_103+518del
ENST00000400519.6:c.103+514_103+518del ENSP00000383363.1:n.103+514_103+518del
ENST00000400521.6:c.103+514_103+518del ENSP00000383365.1:n.103+514_103+518del
ENST00000400525.6:c.103+514_103+518del ENSP00000383369.3:n.103+514_103+518del
ENST00000474308.5:c.103+514_103+518del ENSP00000485665.1:n.103+514_103+518del
ENST00000496729.2:n.108+514_108+518del
NM_001282512.1:c.103+514_103+518del NP_001269441.1:n.103+514_103+518del
NM_006440.4:c.103+514_103+518del NP_006431.2:n.103+514_103+518del
NM_001282512.2:c.103+514_103+518del NP_001269441.1:n.103+514_103+518del
NM_001352300.1:c.103+514_103+518del NP_001339229.1:n.103+514_103+518del
NR_147957.1:n.292+514_292+518del
NM_006440.5:c.103+514_103+518del MANE Select NP_006431.2:n.103+514_103+518del
NM_001282512.3:c.103+514_103+518del NP_001269441.1:n.103+514_103+518del
NM_001352300.2:c.103+514_103+518del NP_001339229.1:n.103+514_103+518del
NR_147957.2:n.118+514_118+518del