Canonical Allele Identifier: CA372495877
Community Standard Title: NM_078480.3(PUF60):c.274C>T (p.Gln92Ter)
Gene: PUF60 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.143821620G>A , CM000670.2:g.143821620G>A GRCh38
NC_000008.9:g.144975778G>A NCBI36
NG_033879.1:g.12767C>T

Transcript Alleles

HGVS Amino-acid Change
NM_078480.3:c.274C>T MANE Select NP_510965.1:p.Gln92Ter
ENST00000526683.6:c.274C>T MANE Select ENSP00000434359.1:p.Gln92Ter
NM_001136033.2:c.145C>T NP_001129505.1:p.Gln49Ter
NM_001136033.3:c.145C>T NP_001129505.1:p.Gln49Ter
NM_001271096.1:c.271C>T NP_001258025.1:p.Gln91Ter
NM_001271096.2:c.271C>T NP_001258025.1:p.Gln91Ter
NM_001271097.1:c.187C>T NP_001258026.1:p.Gln63Ter
NM_001271097.2:c.187C>T NP_001258026.1:p.Gln63Ter
NM_001271098.1:c.271C>T NP_001258027.1:p.Gln91Ter
NM_001271098.2:c.271C>T NP_001258027.1:p.Gln91Ter
NM_001271099.1:c.187C>T NP_001258028.1:p.Gln63Ter
NM_001271099.2:c.187C>T NP_001258028.1:p.Gln63Ter
NM_001271100.1:c.145C>T NP_001258029.1:p.Gln49Ter
NM_001271100.2:c.145C>T NP_001258029.1:p.Gln49Ter
NM_001362895.1:c.385C>T NP_001349824.1:p.Gln129Ter
NM_001362895.2:c.385C>T NP_001349824.1:p.Gln129Ter
NM_001362896.1:c.385C>T NP_001349825.1:p.Gln129Ter
NM_001362896.2:c.385C>T NP_001349825.1:p.Gln129Ter
NM_001362897.1:c.385C>T NP_001349826.1:p.Gln129Ter
NM_001362897.2:c.385C>T NP_001349826.1:p.Gln129Ter
NM_014281.4:c.274C>T NP_055096.2:p.Gln92Ter
NM_014281.5:c.274C>T NP_055096.2:p.Gln92Ter
NM_078480.2:c.274C>T NP_510965.1:p.Gln92Ter
ENST00000313352.11:c.145C>T ENSP00000322016.7:p.Gln49Ter
ENST00000349157.10:c.274C>T ENSP00000322036.7:p.Gln92Ter
ENST00000453551.6:c.145C>T ENSP00000402953.2:p.Gln49Ter
ENST00000456095.6:c.187C>T ENSP00000395417.2:p.Gln63Ter
ENST00000524570.5:n.960C>T
ENST00000524570.6:n.972C>T
ENST00000526151.5:n.286C>T
ENST00000526151.6:n.305C>T
ENST00000526459.5:c.271C>T ENSP00000432610.1:p.Gln91Ter
ENST00000526459.6:c.271C>T ENSP00000432610.2:p.Gln91Ter
ENST00000526683.5:c.274C>T ENSP00000434359.1:p.Gln92Ter
ENST00000527197.5:c.187C>T ENSP00000431960.1:p.Gln63Ter
ENST00000527584.5:n.311C>T
ENST00000527744.5:c.267C>T
ENST00000527744.6:c.271C>T ENSP00000436131.2:p.Gln91Ter
ENST00000528320.5:n.250C>T
ENST00000529999.5:c.385C>T ENSP00000434863.1:p.Gln129Ter
ENST00000531897.5:c.385C>T ENSP00000437309.1:p.Gln129Ter
ENST00000531951.5:n.434C>T
ENST00000531951.6:c.145C>T ENSP00000515500.1:p.Gln49Ter
ENST00000531995.1:n.124C>T
ENST00000532127.5:n.290C>T
ENST00000532127.6:c.274C>T ENSP00000515484.1:p.Gln92Ter
ENST00000533162.1:c.385C>T ENSP00000433403.1:p.Gln129Ter
ENST00000533162.2:c.385C>T ENSP00000433403.2:p.Gln129Ter
ENST00000533362.1:n.593C>T
ENST00000533362.2:c.349C>T ENSP00000515502.1:p.Gln117Ter
ENST00000703744.1:n.1036C>T
ENST00000703803.1:n.422C>T
ENST00000703846.1:c.145C>T ENSP00000515498.1:p.Gln49Ter
ENST00000703847.1:c.385C>T ENSP00000515499.1:p.Gln129Ter
ENST00000703848.1:n.305C>T
ENST00000703849.1:c.145C>T ENSP00000515501.1:p.Gln49Ter
ENST00000703850.1:c.349C>T ENSP00000515503.1:p.Gln117Ter
ENST00000703851.1:n.194C>T
ENST00000703852.1:c.*248C>T ENSP00000515504.1:n.*248C>T
ENST00000703853.1:n.188C>T
ENST00000703866.1:c.274C>T ENSP00000515511.1:p.Gln92Ter
XM_011516929.1:c.385C>T XP_011515231.1:p.Gln129Ter
XM_011516930.1:c.385C>T XP_011515232.1:p.Gln129Ter
XM_017013234.1:c.385C>T XP_016868723.1:p.Gln129Ter
XM_017013235.1:c.349C>T XP_016868724.1:p.Gln117Ter
XM_017013236.1:c.385C>T XP_016868725.1:p.Gln129Ter
XM_017013239.1:c.145C>T XP_016868728.1:p.Gln49Ter
XM_017013240.1:c.145C>T XP_016868729.1:p.Gln49Ter