Canonical Allele Identifier: CA2655325685
Gene: TXNRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19895500del , CM000684.2:g.19895500del GRCh38
NC_000022.10:g.19883023del , CM000684.1:g.19883023del GRCh37
NC_000022.9:g.18263023del NCBI36
NG_011835.1:g.51337del , LRG_417:g.51337del

Transcript Alleles

HGVS Amino-acid change
ENST00000400521.7:c.856del MANE Select ENSP00000383365.1:p.Arg286GlyfsTer?
ENST00000334363.14:c.856del ENSP00000334451.9:p.Arg286GlyfsTer?
ENST00000400518.5:c.766del ENSP00000383362.1:p.Arg256GlyfsTer?
ENST00000400519.6:c.853del ENSP00000383363.1:p.Arg285GlyfsTer?
ENST00000400521.6:c.856del ENSP00000383365.1:p.Arg286GlyfsTer?
ENST00000400525.6:c.787del ENSP00000383369.3:p.Arg263GlyfsTer?
ENST00000474308.5:c.799del ENSP00000485665.1:p.Arg267GlyfsTer?
ENST00000475995.3:c.353del
ENST00000491939.6:c.760del ENSP00000485543.1:p.Arg254GlyfsTer?
ENST00000494454.5:n.930del
ENST00000542719.6:c.568del ENSP00000485128.2:p.Arg190GlyfsTer?
ENST00000634537.1:c.85del ENSP00000489208.1:p.Arg29GlyfsTer?
ENST00000635155.1:n.442del
NM_001282512.1:c.856del NP_001269441.1:p.Arg286GlyfsTer?
NM_006440.4:c.856del NP_006431.2:p.Arg286GlyfsTer?
NM_001282512.2:c.856del NP_001269441.1:p.Arg286GlyfsTer?
NM_001352300.1:c.853del NP_001339229.1:p.Arg285GlyfsTer?
NM_001352301.1:c.766del NP_001339230.1:p.Arg256GlyfsTer?
NM_001352302.1:c.568del NP_001339231.1:p.Arg190GlyfsTer?
NM_001352303.1:c.760del NP_001339232.1:p.Arg254GlyfsTer?
NR_147957.1:n.988del
NM_006440.5:c.856del MANE Select NP_006431.2:p.Arg286GlyfsTer?
NM_001282512.3:c.856del NP_001269441.1:p.Arg286GlyfsTer?
NM_001352300.2:c.853del NP_001339229.1:p.Arg285GlyfsTer?
NR_147957.2:n.814del
NM_001352301.2:c.766del NP_001339230.1:p.Arg256GlyfsTer?
NM_001352302.2:c.568del NP_001339231.1:p.Arg190GlyfsTer?
NM_001352303.2:c.760del NP_001339232.1:p.Arg254GlyfsTer?