Canonical Allele Identifier: CA1825989195
Gene: PUF60 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.143818326G= , CM000670.2:g.143818326G= GRCh38
NC_000008.9:g.144972484G= NCBI36
NG_030583.1:g.2054C=
NG_033879.1:g.16061C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524570.6:n.1209-41C=
ENST00000526151.6:n.2566-41C=
ENST00000526459.6:c.457-41C= ENSP00000432610.2:n.457-41C=
ENST00000527744.6:c.508-41C= ENSP00000436131.2:n.508-41C=
ENST00000531951.6:c.382-41C= ENSP00000515500.1:n.382-41C=
ENST00000532127.6:c.*356-41C= ENSP00000515484.1:n.*356-41C=
ENST00000533162.2:c.622-41C= ENSP00000433403.2:n.622-41C=
ENST00000533362.2:c.586-41C= ENSP00000515502.1:n.586-41C=
ENST00000703744.1:n.1222-41C=
ENST00000703803.1:n.659-41C=
ENST00000703846.1:c.382-41C= ENSP00000515498.1:n.382-41C=
ENST00000703847.1:c.622-41C= ENSP00000515499.1:n.622-41C=
ENST00000703848.1:n.542-41C=
ENST00000703849.1:c.382-41C= ENSP00000515501.1:n.382-41C=
ENST00000703850.1:c.586-41C= ENSP00000515503.1:n.586-41C=
ENST00000703851.1:n.431-41C=
ENST00000703852.1:c.*434-41C= ENSP00000515504.1:n.*434-41C=
ENST00000703853.1:n.425-41C=
ENST00000703866.1:c.511-41C= ENSP00000515511.1:n.511-41C=
ENST00000526683.6:c.511-41C= MANE Select ENSP00000434359.1:n.511-41C=
ENST00000313352.11:c.331-41C= ENSP00000322016.7:n.331-41C=
ENST00000349157.10:c.460-41C= ENSP00000322036.7:n.460-41C=
ENST00000453551.6:c.382-41C= ENSP00000402953.2:n.382-41C=
ENST00000456095.6:c.424-41C= ENSP00000395417.2:n.424-41C=
ENST00000524570.5:n.1197-41C=
ENST00000526459.5:c.457-41C= ENSP00000432610.1:n.457-41C=
ENST00000526683.5:c.511-41C= ENSP00000434359.1:n.511-41C=
ENST00000527197.5:c.373-41C= ENSP00000431960.1:n.373-41C=
ENST00000527744.5:c.504-41C=
ENST00000528320.5:n.482C=
ENST00000528999.5:n.242-41C=
ENST00000529693.1:n.592-41C=
ENST00000529999.5:c.571-41C= ENSP00000434863.1:n.571-41C=
ENST00000531897.5:c.571-41C= ENSP00000437309.1:n.571-41C=
ENST00000531951.5:n.671-41C=
ENST00000532884.1:c.105-41C=
ENST00000533162.1:c.622-41C= ENSP00000433403.1:n.622-41C=
NM_001136033.2:c.382-41C= NP_001129505.1:n.382-41C=
NM_001271096.1:c.457-41C= NP_001258025.1:n.457-41C=
NM_001271097.1:c.373-41C= NP_001258026.1:n.373-41C=
NM_001271098.1:c.508-41C= NP_001258027.1:n.508-41C=
NM_001271099.1:c.424-41C= NP_001258028.1:n.424-41C=
NM_001271100.1:c.331-41C= NP_001258029.1:n.331-41C=
NM_014281.4:c.460-41C= NP_055096.2:n.460-41C=
NM_078480.2:c.511-41C= NP_510965.1:n.511-41C=
XM_011516929.1:c.622-41C= XP_011515231.1:n.622-41C=
XM_011516930.1:c.571-41C= XP_011515232.1:n.571-41C=
NM_001362895.1:c.622-41C= NP_001349824.1:n.622-41C=
NM_001362896.1:c.622-41C= NP_001349825.1:n.622-41C=
NM_001362897.1:c.571-41C= NP_001349826.1:n.571-41C=
XM_017013234.1:c.622-41C= XP_016868723.1:n.622-41C=
XM_017013235.1:c.586-41C= XP_016868724.1:n.586-41C=
XM_017013236.1:c.571-41C= XP_016868725.1:n.571-41C=
XM_017013239.1:c.382-41C= XP_016868728.1:n.382-41C=
XM_017013240.1:c.331-41C= XP_016868729.1:n.331-41C=
NM_001136033.3:c.382-41C= NP_001129505.1:n.382-41C=
NM_001271096.2:c.457-41C= NP_001258025.1:n.457-41C=
NM_001271097.2:c.373-41C= NP_001258026.1:n.373-41C=
NM_001271098.2:c.508-41C= NP_001258027.1:n.508-41C=
NM_001271099.2:c.424-41C= NP_001258028.1:n.424-41C=
NM_001271100.2:c.331-41C= NP_001258029.1:n.331-41C=
NM_001362895.2:c.622-41C= NP_001349824.1:n.622-41C=
NM_001362896.2:c.622-41C= NP_001349825.1:n.622-41C=
NM_001362897.2:c.571-41C= NP_001349826.1:n.571-41C=
NM_014281.5:c.460-41C= NP_055096.2:n.460-41C=
NM_078480.3:c.511-41C= MANE Select NP_510965.1:n.511-41C=