Canonical Allele Identifier: CA2655329353
Gene: TXNRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19918905del , CM000684.2:g.19918905del GRCh38
NC_000022.10:g.19906428del , CM000684.1:g.19906428del GRCh37
NC_000022.9:g.18286428del NCBI36
NG_011835.1:g.27936del , LRG_417:g.27936del

Transcript Alleles

HGVS Amino-acid change
ENST00000400521.7:c.333del MANE Select ENSP00000383365.1:p.Asn112ThrfsTer25
ENST00000334363.14:c.333del ENSP00000334451.9:p.Asn112ThrfsTer25
ENST00000400518.5:c.243del ENSP00000383362.1:p.Asn82ThrfsTer25
ENST00000400519.6:c.330del ENSP00000383363.1:p.Asn111ThrfsTer25
ENST00000400521.6:c.333del ENSP00000383365.1:p.Asn112ThrfsTer25
ENST00000400525.6:c.264del ENSP00000383369.3:p.Asn89ThrfsTer25
ENST00000474308.5:c.276del ENSP00000485665.1:p.Asn93ThrfsTer25
ENST00000491939.6:c.237del ENSP00000485543.1:p.Asn80ThrfsTer25
ENST00000496729.2:n.338del
ENST00000542719.6:c.45del ENSP00000485128.2:p.Asn16ThrfsTer25
NM_001282512.1:c.333del NP_001269441.1:p.Asn112ThrfsTer25
NM_006440.4:c.333del NP_006431.2:p.Asn112ThrfsTer25
NM_001282512.2:c.333del NP_001269441.1:p.Asn112ThrfsTer25
NM_001352300.1:c.330del NP_001339229.1:p.Asn111ThrfsTer25
NM_001352301.1:c.243del NP_001339230.1:p.Asn82ThrfsTer25
NM_001352302.1:c.45del NP_001339231.1:p.Asn16ThrfsTer25
NM_001352303.1:c.237del NP_001339232.1:p.Asn80ThrfsTer25
NR_147957.1:n.465del
NM_006440.5:c.333del MANE Select NP_006431.2:p.Asn112ThrfsTer25
NM_001282512.3:c.333del NP_001269441.1:p.Asn112ThrfsTer25
NM_001352300.2:c.330del NP_001339229.1:p.Asn111ThrfsTer25
NR_147957.2:n.291del
NM_001352301.2:c.243del NP_001339230.1:p.Asn82ThrfsTer25
NM_001352302.2:c.45del NP_001339231.1:p.Asn16ThrfsTer25
NM_001352303.2:c.237del NP_001339232.1:p.Asn80ThrfsTer25