Canonical Allele Identifier: CA1576971570
Gene: TNFAIP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119393713_119393714delinsAT , CM000667.2:g.119393713_119393714delinsAT GRCh38
NC_000005.9:g.118729408_118729409delinsAT , CM000667.1:g.118729408_118729409delinsAT GRCh37
NC_000005.8:g.118757307_118757308delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000504771.3:c.*332_*333delinsAT MANE Select ENSP00000422245.1:n.*332_*333delinsAT
ENST00000415806.2:c.*928_*929delinsAT ENSP00000408534.2:n.*928_*929delinsAT
ENST00000503646.1:c.*332_*333delinsAT ENSP00000421848.1:n.*332_*333delinsAT
ENST00000504771.2:c.*332_*333delinsAT ENSP00000422245.1:n.*332_*333delinsAT
ENST00000513374.1:c.*332_*333delinsAT ENSP00000427424.1:n.*332_*333delinsAT
NM_001077654.2:c.*332_*333delinsAT NP_001071122.1:n.*332_*333delinsAT
NM_001286813.1:c.*332_*333delinsAT NP_001273742.1:n.*332_*333delinsAT
NM_001286814.1:c.*332_*333delinsAT NP_001273743.1:n.*332_*333delinsAT
NM_001286815.1:c.*332_*333delinsAT NP_001273744.1:n.*332_*333delinsAT
NM_001286817.1:c.*332_*333delinsAT NP_001273746.1:n.*332_*333delinsAT
NM_014350.3:c.*332_*333delinsAT NP_055165.2:n.*332_*333delinsAT
XM_017009327.1:c.*332_*333delinsAT XP_016864816.1:n.*332_*333delinsAT
XM_017009328.1:c.*332_*333delinsAT XP_016864817.1:n.*332_*333delinsAT
NM_014350.4:c.*332_*333delinsAT MANE Select NP_055165.2:n.*332_*333delinsAT
NM_001077654.3:c.*332_*333delinsAT NP_001071122.1:n.*332_*333delinsAT
NM_001286813.2:c.*332_*333delinsAT NP_001273742.1:n.*332_*333delinsAT
NM_001286815.2:c.*332_*333delinsAT NP_001273744.1:n.*332_*333delinsAT
NM_001286817.2:c.*332_*333delinsAT NP_001273746.1:n.*332_*333delinsAT