Canonical Allele Identifier: CA1825988538
Gene: PUF60 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.143817680A= , CM000670.2:g.143817680A= GRCh38
NC_000008.9:g.144971838A= NCBI36
NG_030583.1:g.2700T=
NG_033879.1:g.16707T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524570.6:n.1618T=
ENST00000526151.6:n.2975T=
ENST00000526459.6:c.866T= ENSP00000432610.2:p.Met289=
ENST00000527744.6:c.917T= ENSP00000436131.2:p.Met306=
ENST00000531951.6:c.791T= ENSP00000515500.1:p.Met264=
ENST00000532127.6:c.*765T= ENSP00000515484.1:n.*765T=
ENST00000533162.2:c.1031T= ENSP00000433403.2:p.Met344=
ENST00000533362.2:c.995T= ENSP00000515502.1:p.Met332=
ENST00000703744.1:n.1631T=
ENST00000703803.1:n.1185T=
ENST00000703846.1:c.791T= ENSP00000515498.1:p.Met264=
ENST00000703847.1:c.1031T= ENSP00000515499.1:p.Met344=
ENST00000703848.1:n.951T=
ENST00000703849.1:c.791T= ENSP00000515501.1:p.Met264=
ENST00000703850.1:c.995T= ENSP00000515503.1:p.Met332=
ENST00000703851.1:n.840T=
ENST00000703866.1:c.920T= ENSP00000515511.1:p.Met307=
ENST00000526683.6:c.920T= MANE Select ENSP00000434359.1:p.Met307=
ENST00000313352.11:c.740T= ENSP00000322016.7:p.Met247=
ENST00000349157.10:c.869T= ENSP00000322036.7:p.Met290=
ENST00000453551.6:c.791T= ENSP00000402953.2:p.Met264=
ENST00000456095.6:c.833T= ENSP00000395417.2:p.Met278=
ENST00000524570.5:n.1606T=
ENST00000526459.5:c.866T= ENSP00000432610.1:p.Met289=
ENST00000526683.5:c.920T= ENSP00000434359.1:p.Met307=
ENST00000527197.5:c.782T= ENSP00000431960.1:p.Met261=
ENST00000527744.5:c.913T=
ENST00000532884.1:c.529T=
NM_001136033.2:c.791T= NP_001129505.1:p.Met264=
NM_001271096.1:c.866T= NP_001258025.1:p.Met289=
NM_001271097.1:c.782T= NP_001258026.1:p.Met261=
NM_001271098.1:c.917T= NP_001258027.1:p.Met306=
NM_001271099.1:c.833T= NP_001258028.1:p.Met278=
NM_001271100.1:c.740T= NP_001258029.1:p.Met247=
NM_014281.4:c.869T= NP_055096.2:p.Met290=
NM_078480.2:c.920T= NP_510965.1:p.Met307=
XM_011516929.1:c.1031T= XP_011515231.1:p.Met344=
XM_011516930.1:c.980T= XP_011515232.1:p.Met327=
NM_001362895.1:c.1031T= NP_001349824.1:p.Met344=
NM_001362896.1:c.1031T= NP_001349825.1:p.Met344=
NM_001362897.1:c.980T= NP_001349826.1:p.Met327=
XM_017013234.1:c.1031T= XP_016868723.1:p.Met344=
XM_017013235.1:c.995T= XP_016868724.1:p.Met332=
XM_017013236.1:c.980T= XP_016868725.1:p.Met327=
XM_017013239.1:c.791T= XP_016868728.1:p.Met264=
XM_017013240.1:c.740T= XP_016868729.1:p.Met247=
NM_001136033.3:c.791T= NP_001129505.1:p.Met264=
NM_001271096.2:c.866T= NP_001258025.1:p.Met289=
NM_001271097.2:c.782T= NP_001258026.1:p.Met261=
NM_001271098.2:c.917T= NP_001258027.1:p.Met306=
NM_001271099.2:c.833T= NP_001258028.1:p.Met278=
NM_001271100.2:c.740T= NP_001258029.1:p.Met247=
NM_001362895.2:c.1031T= NP_001349824.1:p.Met344=
NM_001362896.2:c.1031T= NP_001349825.1:p.Met344=
NM_001362897.2:c.980T= NP_001349826.1:p.Met327=
NM_014281.5:c.869T= NP_055096.2:p.Met290=
NM_078480.3:c.920T= MANE Select NP_510965.1:p.Met307=