Canonical Allele Identifier: CA347916
Gene: TNFAIP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.137876162del , CM000668.2:g.137876162del GRCh38
NC_000006.11:g.138197299del , CM000668.1:g.138197299del GRCh37
NC_000006.10:g.138238992del NCBI36
NG_032761.1:g.13719del

Transcript Alleles

HGVS Amino-acid Change
ENST00000420009.6:c.801del ENSP00000401562.2:p.Pro268LeufsTer19
ENST00000711061.1:c.*524del ENSP00000518561.1:n.*524del
ENST00000421450.2:c.801del ENSP00000393577.2:p.Pro268LeufsTer19
ENST00000433680.2:c.801del ENSP00000409845.2:p.Pro268LeufsTer19
ENST00000485192.2:n.1422del
ENST00000698329.1:n.1150del
ENST00000698330.1:n.296-2270del
ENST00000612899.5:c.801del MANE Select ENSP00000481570.1:p.Pro268LeufsTer19
ENST00000237289.8:c.801del ENSP00000237289.4:p.Pro268LeufsTer19
ENST00000485192.1:n.325del
ENST00000612899.4:c.801del ENSP00000481570.1:p.Pro268LeufsTer19
ENST00000614035.4:c.801del ENSP00000481122.2:p.Pro268LeufsTer19
ENST00000615468.4:c.*155del ENSP00000479556.1:n.*155del
ENST00000619035.4:c.801del ENSP00000478438.1:p.Pro268LeufsTer19
ENST00000620204.3:c.801del ENSP00000481454.1:p.Pro268LeufsTer19
ENST00000621150.3:c.801del ENSP00000484332.2:p.Pro268LeufsTer19
NM_001270507.1:c.801del NP_001257436.1:p.Pro268LeufsTer19
NM_001270508.1:c.801del NP_001257437.1:p.Pro268LeufsTer19
NM_006290.3:c.801del NP_006281.1:p.Pro268LeufsTer19
XM_005267119.1:c.801del XP_005267176.1:p.Pro268LeufsTer19
XM_006715555.1:c.162del XP_006715618.1:p.Pro55LeufsTer19
XM_011536095.1:c.801del XP_011534397.1:p.Pro268LeufsTer19
XM_011536096.1:c.801del XP_011534398.1:p.Pro268LeufsTer19
XM_011536096.2:c.801del XP_011534398.1:p.Pro268LeufsTer19
XM_024446532.1:c.801del XP_024302300.1:p.Pro268LeufsTer19
XM_024446533.1:c.801del XP_024302301.1:p.Pro268LeufsTer19
NM_001270508.2:c.801del MANE Select NP_001257437.1:p.Pro268LeufsTer19
NM_001270507.2:c.801del NP_001257436.1:p.Pro268LeufsTer19
NM_006290.4:c.801del NP_006281.1:p.Pro268LeufsTer19