Canonical Allele Identifier: CA5448251
Community Standard Title: NM_014915.3(ANKRD26):c.2329_2332del (p.Leu777SerfsTer14)
Gene: ANKRD26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.27040010_27040013del , CM000672.2:g.27040010_27040013del GRCh38
NC_000010.10:g.27328939_27328942del , CM000672.1:g.27328939_27328942del GRCh37
NC_000010.9:g.27368945_27368948del NCBI36
NG_031973.2:g.65488_65491del , LRG_605:g.65488_65491del

Transcript Alleles

HGVS Amino-acid Change
NM_014915.3:c.2329_2332del MANE Select NP_055730.2:p.Leu777SerfsTer14
ENST00000376087.5:c.2329_2332del MANE Select ENSP00000365255.4:p.Leu777SerfsTer14
NM_001256053.1:c.2326_2329del NP_001242982.1:p.Leu776SerfsTer14
NM_001256053.2:c.2326_2329del NP_001242982.1:p.Leu776SerfsTer14
NM_014915.2:c.2329_2332del , LRG_605t1:c.2329_2332del NP_055730.2:p.Leu777SerfsTer14
ENST00000376087.4:c.2329_2332del ENSP00000365255.4:p.Leu777SerfsTer14
ENST00000436985.6:c.2377_2380del ENSP00000405112.2:p.Leu793SerfsTer14
ENST00000436985.7:c.2326_2329del ENSP00000405112.3:p.Leu776SerfsTer14
ENST00000490015.1:n.527_530del
ENST00000675187.1:c.*1665_*1668del ENSP00000502611.1:n.*1665_*1668del
ENST00000675349.1:n.2058_2061del
ENST00000676232.1:c.2037_2040del
ENST00000676420.1:c.*2146_*2149del ENSP00000502355.1:n.*2146_*2149del
XM_006717423.2:c.3415_3418del XP_006717486.1:p.Leu1139SerfsTer14
XM_006717424.2:c.3412_3415del XP_006717487.1:p.Leu1138SerfsTer14
XM_006717425.2:c.3415_3418del XP_006717488.1:p.Leu1139SerfsTer14
XM_006717425.4:c.3415_3418del XP_006717488.1:p.Leu1139SerfsTer14
XM_006717427.2:c.2572_2575del XP_006717490.1:p.Leu858SerfsTer14
XM_006717428.2:c.2230_2233del XP_006717491.1:p.Leu744SerfsTer14
XM_011519415.1:c.3403_3406del XP_011517717.1:p.Leu1135SerfsTer14
XM_011519416.1:c.3415_3418del XP_011517718.1:p.Leu1139SerfsTer14
XM_011519416.2:c.3415_3418del XP_011517718.1:p.Leu1139SerfsTer14
XM_011519417.1:c.3415_3418del XP_011517719.1:p.Leu1139SerfsTer14
XM_011519418.1:c.3415_3418del XP_011517720.1:p.Leu1139SerfsTer14
XM_011519419.1:c.3316_3319del XP_011517721.1:p.Leu1106SerfsTer14
XM_011519420.1:c.3415_3418del XP_011517722.1:p.Leu1139SerfsTer14
XM_011519421.1:c.2572_2575del XP_011517723.1:p.Leu858SerfsTer14
XM_011519422.1:c.3415_3418del XP_011517724.1:p.Leu1139SerfsTer14
XM_011519423.1:c.2572_2575del XP_011517725.1:p.Leu858SerfsTer14
XM_011519424.1:c.2029_2032del XP_011517726.1:p.Leu677SerfsTer14
XM_011519425.1:c.3415_3418del XP_011517727.1:p.Leu1139SerfsTer14
XM_017015928.1:c.3415_3418del XP_016871417.1:p.Leu1139SerfsTer14
XM_017015929.1:c.3403_3406del XP_016871418.1:p.Leu1135SerfsTer14
XM_017015930.1:c.3415_3418del XP_016871419.1:p.Leu1139SerfsTer14
XM_017015931.1:c.3415_3418del XP_016871420.1:p.Leu1139SerfsTer14
XM_017015932.1:c.3415_3418del XP_016871421.1:p.Leu1139SerfsTer14
XM_017015933.1:c.3415_3418del XP_016871422.1:p.Leu1139SerfsTer14
XR_930483.1:n.3587_3590del
XR_930484.1:n.3587_3590del