Canonical Allele Identifier: CA347924
Gene: TNFAIP3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.137879254del , CM000668.2:g.137879254del GRCh38
NC_000006.11:g.138200391del , CM000668.1:g.138200391del GRCh37
NC_000006.10:g.138242084del NCBI36
NG_032761.1:g.16811del

Transcript Alleles

HGVS Amino-acid Change
ENST00000420009.6:c.1809del ENSP00000401562.2:p.Thr604ArgfsTer?
ENST00000711061.1:c.*1532del ENSP00000518561.1:n.*1532del
ENST00000421450.2:c.1809del ENSP00000393577.2:p.Thr604ArgfsTer?
ENST00000433680.2:c.1809del ENSP00000409845.2:p.Thr604ArgfsTer?
ENST00000485192.2:n.2430del
ENST00000698329.1:n.2158del
ENST00000612899.5:c.1809del MANE Select ENSP00000481570.1:p.Thr604ArgfsTer?
ENST00000237289.8:c.1809del ENSP00000237289.4:p.Thr604ArgfsTer?
ENST00000612899.4:c.1809del ENSP00000481570.1:p.Thr604ArgfsTer?
ENST00000615468.4:c.*1163del ENSP00000479556.1:n.*1163del
ENST00000619035.4:c.1809del ENSP00000478438.1:p.Thr604ArgfsTer?
ENST00000620204.3:c.1809del ENSP00000481454.1:p.Thr604ArgfsTer?
NM_001270507.1:c.1809del NP_001257436.1:p.Thr604ArgfsTer?
NM_001270508.1:c.1809del NP_001257437.1:p.Thr604ArgfsTer?
NM_006290.3:c.1809del NP_006281.1:p.Thr604ArgfsTer?
XM_005267119.1:c.1809del XP_005267176.1:p.Thr604ArgfsTer?
XM_006715555.1:c.1170del XP_006715618.1:p.Thr391ArgfsTer?
XM_011536095.1:c.1809del XP_011534397.1:p.Thr604ArgfsTer?
XM_011536096.1:c.1809del XP_011534398.1:p.Thr604ArgfsTer?
XM_011536096.2:c.1809del XP_011534398.1:p.Thr604ArgfsTer?
XM_024446532.1:c.1809del XP_024302300.1:p.Thr604ArgfsTer?
XM_024446533.1:c.1809del XP_024302301.1:p.Thr604ArgfsTer?
NM_001270508.2:c.1809del MANE Select NP_001257437.1:p.Thr604ArgfsTer?
NM_001270507.2:c.1809del NP_001257436.1:p.Thr604ArgfsTer?
NM_006290.4:c.1809del NP_006281.1:p.Thr604ArgfsTer?
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