Canonical Allele Identifier: CA1825988485
Gene: PUF60 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.143817618C= , CM000670.2:g.143817618C= GRCh38
NC_000008.9:g.144971776C= NCBI36
NG_030583.1:g.2762G=
NG_033879.1:g.16769G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524570.6:n.1680G=
ENST00000526151.6:n.3037G=
ENST00000526459.6:c.928G= ENSP00000432610.2:p.Ala310=
ENST00000527744.6:c.979G= ENSP00000436131.2:p.Ala327=
ENST00000531951.6:c.853G= ENSP00000515500.1:p.Ala285=
ENST00000532127.6:c.*827G= ENSP00000515484.1:n.*827G=
ENST00000533162.2:c.1093G= ENSP00000433403.2:p.Ala365=
ENST00000533362.2:c.1057G= ENSP00000515502.1:p.Ala353=
ENST00000703744.1:n.1693G=
ENST00000703803.1:n.1247G=
ENST00000703846.1:c.853G= ENSP00000515498.1:p.Ala285=
ENST00000703847.1:c.1093G= ENSP00000515499.1:p.Ala365=
ENST00000703848.1:n.1013G=
ENST00000703849.1:c.853G= ENSP00000515501.1:p.Ala285=
ENST00000703850.1:c.1057G= ENSP00000515503.1:p.Ala353=
ENST00000703851.1:n.902G=
ENST00000703866.1:c.982G= ENSP00000515511.1:p.Ala328=
ENST00000526683.6:c.982G= MANE Select ENSP00000434359.1:p.Ala328=
ENST00000313352.11:c.802G= ENSP00000322016.7:p.Ala268=
ENST00000349157.10:c.931G= ENSP00000322036.7:p.Ala311=
ENST00000453551.6:c.853G= ENSP00000402953.2:p.Ala285=
ENST00000456095.6:c.895G= ENSP00000395417.2:p.Ala299=
ENST00000524570.5:n.1668G=
ENST00000526459.5:c.928G= ENSP00000432610.1:p.Ala310=
ENST00000526683.5:c.982G= ENSP00000434359.1:p.Ala328=
ENST00000527197.5:c.844G= ENSP00000431960.1:p.Ala282=
ENST00000527744.5:c.975G=
ENST00000532884.1:c.591G=
NM_001136033.2:c.853G= NP_001129505.1:p.Ala285=
NM_001271096.1:c.928G= NP_001258025.1:p.Ala310=
NM_001271097.1:c.844G= NP_001258026.1:p.Ala282=
NM_001271098.1:c.979G= NP_001258027.1:p.Ala327=
NM_001271099.1:c.895G= NP_001258028.1:p.Ala299=
NM_001271100.1:c.802G= NP_001258029.1:p.Ala268=
NM_014281.4:c.931G= NP_055096.2:p.Ala311=
NM_078480.2:c.982G= NP_510965.1:p.Ala328=
XM_011516929.1:c.1093G= XP_011515231.1:p.Ala365=
XM_011516930.1:c.1042G= XP_011515232.1:p.Ala348=
NM_001362895.1:c.1093G= NP_001349824.1:p.Ala365=
NM_001362896.1:c.1093G= NP_001349825.1:p.Ala365=
NM_001362897.1:c.1042G= NP_001349826.1:p.Ala348=
XM_017013234.1:c.1093G= XP_016868723.1:p.Ala365=
XM_017013235.1:c.1057G= XP_016868724.1:p.Ala353=
XM_017013236.1:c.1042G= XP_016868725.1:p.Ala348=
XM_017013239.1:c.853G= XP_016868728.1:p.Ala285=
XM_017013240.1:c.802G= XP_016868729.1:p.Ala268=
NM_001136033.3:c.853G= NP_001129505.1:p.Ala285=
NM_001271096.2:c.928G= NP_001258025.1:p.Ala310=
NM_001271097.2:c.844G= NP_001258026.1:p.Ala282=
NM_001271098.2:c.979G= NP_001258027.1:p.Ala327=
NM_001271099.2:c.895G= NP_001258028.1:p.Ala299=
NM_001271100.2:c.802G= NP_001258029.1:p.Ala268=
NM_001362895.2:c.1093G= NP_001349824.1:p.Ala365=
NM_001362896.2:c.1093G= NP_001349825.1:p.Ala365=
NM_001362897.2:c.1042G= NP_001349826.1:p.Ala348=
NM_014281.5:c.931G= NP_055096.2:p.Ala311=
NM_078480.3:c.982G= MANE Select NP_510965.1:p.Ala328=