Canonical Allele Identifier: CA5447643
Community Standard Title: NM_014915.3(ANKRD26):c.5099_5100del (p.Tyr1700CysfsTer?)
Gene: ANKRD26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.27005625_27005626del , CM000672.2:g.27005625_27005626del GRCh38
NC_000010.10:g.27294554_27294555del , CM000672.1:g.27294554_27294555del GRCh37
NC_000010.9:g.27334560_27334561del NCBI36
NG_031973.2:g.99875_99876del , LRG_605:g.99875_99876del

Transcript Alleles

HGVS Amino-acid Change
NM_014915.3:c.5099_5100del MANE Select NP_055730.2:p.Tyr1700CysfsTer?
ENST00000376087.5:c.5099_5100del MANE Select ENSP00000365255.4:p.Tyr1700CysfsTer?
NM_001256053.1:c.5096_5097del NP_001242982.1:p.Tyr1699CysfsTer?
NM_001256053.2:c.5096_5097del NP_001242982.1:p.Tyr1699CysfsTer?
NM_014915.2:c.5099_5100del , LRG_605t1:c.5099_5100del NP_055730.2:p.Tyr1700CysfsTer?
ENST00000376087.4:c.5099_5100del ENSP00000365255.4:p.Tyr1700CysfsTer?
ENST00000436985.6:c.5147_5148del ENSP00000405112.2:p.Tyr1716CysfsTer?
ENST00000436985.7:c.5096_5097del ENSP00000405112.3:p.Tyr1699CysfsTer?
ENST00000445828.5:c.561_562del
ENST00000674670.1:c.489+1293_489+1294del
ENST00000675116.1:c.2957_2958del
ENST00000675439.1:c.324+1293_324+1294del
ENST00000675936.1:c.1515_1516del
ENST00000676280.1:c.481_482del
XM_006717423.2:c.6185_6186del XP_006717486.1:p.Tyr2062CysfsTer?
XM_006717424.2:c.6182_6183del XP_006717487.1:p.Tyr2061CysfsTer?
XM_006717425.2:c.6085+1293_6085+1294del XP_006717488.1:n.6085+1293_6085+1294del
XM_006717425.4:c.6085+1293_6085+1294del XP_006717488.1:n.6085+1293_6085+1294del
XM_006717427.2:c.5342_5343del XP_006717490.1:p.Tyr1781CysfsTer?
XM_006717428.2:c.5000_5001del XP_006717491.1:p.Tyr1667CysfsTer?
XM_011519415.1:c.6173_6174del XP_011517717.1:p.Tyr2058CysfsTer?
XM_011519416.1:c.6085+1293_6085+1294del XP_011517718.1:n.6085+1293_6085+1294del
XM_011519416.2:c.6085+1293_6085+1294del XP_011517718.1:n.6085+1293_6085+1294del
XM_011519417.1:c.6085+1293_6085+1294del XP_011517719.1:n.6085+1293_6085+1294del
XM_011519418.1:c.6085+1293_6085+1294del XP_011517720.1:n.6085+1293_6085+1294del
XM_011519419.1:c.6086_6087del XP_011517721.1:p.Tyr2029CysfsTer?
XM_011519420.1:c.5894_5895del XP_011517722.1:p.Tyr1965CysfsTer?
XM_011519421.1:c.5342_5343del XP_011517723.1:p.Tyr1781CysfsTer?
XM_011519423.1:c.5342_5343del XP_011517725.1:p.Tyr1781CysfsTer?
XM_011519424.1:c.4799_4800del XP_011517726.1:p.Tyr1600CysfsTer?
XM_017015928.1:c.6085+1293_6085+1294del XP_016871417.1:n.6085+1293_6085+1294del
XM_017015929.1:c.6073+1293_6073+1294del XP_016871418.1:n.6073+1293_6073+1294del
XM_017015930.1:c.6085+1293_6085+1294del XP_016871419.1:n.6085+1293_6085+1294del
XM_017015931.1:c.6085+1293_6085+1294del XP_016871420.1:n.6085+1293_6085+1294del
XM_017015932.1:c.6085+1293_6085+1294del XP_016871421.1:n.6085+1293_6085+1294del
XM_017015933.1:c.*1422_*1423del XP_016871422.1:n.*1422_*1423del
XR_930483.1:n.6257+1293_6257+1294del
XR_930484.1:n.6257+1293_6257+1294del