Canonical Allele Identifier: CA16618605
Gene: PUF60 HGNC NCBI

Linked Data

dbSNP Id: rs1064794916

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.143816711_143816713del , CM000670.2:g.143816711_143816713del GRCh38
NC_000008.9:g.144970869_144970871del NCBI36
NG_030583.1:g.3672_3674del
NG_033879.1:g.17679_17681del

Transcript Alleles

HGVS Amino-acid change
ENST00000524570.6:n.2190_2192del
ENST00000526151.6:n.3547_3549del
ENST00000526459.6:c.1438_1440del ENSP00000432610.2:p.Ile480del
ENST00000527744.6:c.1489_1491del ENSP00000436131.2:p.Ile497del
ENST00000531951.6:c.1363_1365del ENSP00000515500.1:p.Ile455del
ENST00000532127.6:c.*1337_*1339del ENSP00000515484.1:n.*1337_*1339del
ENST00000533162.2:c.1603_1605del ENSP00000433403.2:p.Ile535del
ENST00000533362.2:c.1567_1569del ENSP00000515502.1:p.Ile523del
ENST00000703744.1:n.2203_2205del
ENST00000703803.1:n.1757_1759del
ENST00000703846.1:c.1363_1365del ENSP00000515498.1:p.Ile455del
ENST00000703847.1:c.1603_1605del ENSP00000515499.1:p.Ile535del
ENST00000703848.1:n.1523_1525del
ENST00000703849.1:c.1363_1365del ENSP00000515501.1:p.Ile455del
ENST00000703850.1:c.1567_1569del ENSP00000515503.1:p.Ile523del
ENST00000703866.1:c.1492_1494del ENSP00000515511.1:p.Ile498del
ENST00000526683.6:c.1492_1494del MANE Select ENSP00000434359.1:p.Ile498del
ENST00000313352.11:c.1312_1314del ENSP00000322016.7:p.Ile438del
ENST00000349157.10:c.1441_1443del ENSP00000322036.7:p.Ile481del
ENST00000453551.6:c.1363_1365del ENSP00000402953.2:p.Ile455del
ENST00000456095.6:c.1405_1407del ENSP00000395417.2:p.Ile469del
ENST00000526683.5:c.1492_1494del ENSP00000434359.1:p.Ile498del
ENST00000527197.5:c.1354_1356del ENSP00000431960.1:p.Ile452del
NM_001136033.2:c.1363_1365del NP_001129505.1:p.Ile455del
NM_001271096.1:c.1438_1440del NP_001258025.1:p.Ile480del
NM_001271097.1:c.1354_1356del NP_001258026.1:p.Ile452del
NM_001271098.1:c.1489_1491del NP_001258027.1:p.Ile497del
NM_001271099.1:c.1405_1407del NP_001258028.1:p.Ile469del
NM_001271100.1:c.1312_1314del NP_001258029.1:p.Ile438del
NM_014281.4:c.1441_1443del NP_055096.2:p.Ile481del
NM_078480.2:c.1492_1494del NP_510965.1:p.Ile498del
XM_011516929.1:c.1603_1605del XP_011515231.1:p.Ile535del
XM_011516930.1:c.1552_1554del XP_011515232.1:p.Ile518del
NM_001362895.1:c.1603_1605del NP_001349824.1:p.Ile535del
NM_001362896.1:c.1603_1605del NP_001349825.1:p.Ile535del
NM_001362897.1:c.1552_1554del NP_001349826.1:p.Ile518del
XM_017013234.1:c.1603_1605del XP_016868723.1:p.Ile535del
XM_017013235.1:c.1567_1569del XP_016868724.1:p.Ile523del
XM_017013236.1:c.1552_1554del XP_016868725.1:p.Ile518del
XM_017013239.1:c.1363_1365del XP_016868728.1:p.Ile455del
XM_017013240.1:c.1312_1314del XP_016868729.1:p.Ile438del
NM_001136033.3:c.1363_1365del NP_001129505.1:p.Ile455del
NM_001271096.2:c.1438_1440del NP_001258025.1:p.Ile480del
NM_001271097.2:c.1354_1356del NP_001258026.1:p.Ile452del
NM_001271098.2:c.1489_1491del NP_001258027.1:p.Ile497del
NM_001271099.2:c.1405_1407del NP_001258028.1:p.Ile469del
NM_001271100.2:c.1312_1314del NP_001258029.1:p.Ile438del
NM_001362895.2:c.1603_1605del NP_001349824.1:p.Ile535del
NM_001362896.2:c.1603_1605del NP_001349825.1:p.Ile535del
NM_001362897.2:c.1552_1554del NP_001349826.1:p.Ile518del
NM_014281.5:c.1441_1443del NP_055096.2:p.Ile481del
NM_078480.3:c.1492_1494del MANE Select NP_510965.1:p.Ile498del