Canonical Allele Identifier: CA1825988492
Gene: PUF60 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.143817623G= , CM000670.2:g.143817623G= GRCh38
NC_000008.9:g.144971781G= NCBI36
NG_030583.1:g.2757C=
NG_033879.1:g.16764C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524570.6:n.1675C=
ENST00000526151.6:n.3032C=
ENST00000526459.6:c.923C= ENSP00000432610.2:p.Ala308=
ENST00000527744.6:c.974C= ENSP00000436131.2:p.Ala325=
ENST00000531951.6:c.848C= ENSP00000515500.1:p.Ala283=
ENST00000532127.6:c.*822C= ENSP00000515484.1:n.*822C=
ENST00000533162.2:c.1088C= ENSP00000433403.2:p.Ala363=
ENST00000533362.2:c.1052C= ENSP00000515502.1:p.Ala351=
ENST00000703744.1:n.1688C=
ENST00000703803.1:n.1242C=
ENST00000703846.1:c.848C= ENSP00000515498.1:p.Ala283=
ENST00000703847.1:c.1088C= ENSP00000515499.1:p.Ala363=
ENST00000703848.1:n.1008C=
ENST00000703849.1:c.848C= ENSP00000515501.1:p.Ala283=
ENST00000703850.1:c.1052C= ENSP00000515503.1:p.Ala351=
ENST00000703851.1:n.897C=
ENST00000703866.1:c.977C= ENSP00000515511.1:p.Ala326=
ENST00000526683.6:c.977C= MANE Select ENSP00000434359.1:p.Ala326=
ENST00000313352.11:c.797C= ENSP00000322016.7:p.Ala266=
ENST00000349157.10:c.926C= ENSP00000322036.7:p.Ala309=
ENST00000453551.6:c.848C= ENSP00000402953.2:p.Ala283=
ENST00000456095.6:c.890C= ENSP00000395417.2:p.Ala297=
ENST00000524570.5:n.1663C=
ENST00000526459.5:c.923C= ENSP00000432610.1:p.Ala308=
ENST00000526683.5:c.977C= ENSP00000434359.1:p.Ala326=
ENST00000527197.5:c.839C= ENSP00000431960.1:p.Ala280=
ENST00000527744.5:c.970C=
ENST00000532884.1:c.586C=
NM_001136033.2:c.848C= NP_001129505.1:p.Ala283=
NM_001271096.1:c.923C= NP_001258025.1:p.Ala308=
NM_001271097.1:c.839C= NP_001258026.1:p.Ala280=
NM_001271098.1:c.974C= NP_001258027.1:p.Ala325=
NM_001271099.1:c.890C= NP_001258028.1:p.Ala297=
NM_001271100.1:c.797C= NP_001258029.1:p.Ala266=
NM_014281.4:c.926C= NP_055096.2:p.Ala309=
NM_078480.2:c.977C= NP_510965.1:p.Ala326=
XM_011516929.1:c.1088C= XP_011515231.1:p.Ala363=
XM_011516930.1:c.1037C= XP_011515232.1:p.Ala346=
NM_001362895.1:c.1088C= NP_001349824.1:p.Ala363=
NM_001362896.1:c.1088C= NP_001349825.1:p.Ala363=
NM_001362897.1:c.1037C= NP_001349826.1:p.Ala346=
XM_017013234.1:c.1088C= XP_016868723.1:p.Ala363=
XM_017013235.1:c.1052C= XP_016868724.1:p.Ala351=
XM_017013236.1:c.1037C= XP_016868725.1:p.Ala346=
XM_017013239.1:c.848C= XP_016868728.1:p.Ala283=
XM_017013240.1:c.797C= XP_016868729.1:p.Ala266=
NM_001136033.3:c.848C= NP_001129505.1:p.Ala283=
NM_001271096.2:c.923C= NP_001258025.1:p.Ala308=
NM_001271097.2:c.839C= NP_001258026.1:p.Ala280=
NM_001271098.2:c.974C= NP_001258027.1:p.Ala325=
NM_001271099.2:c.890C= NP_001258028.1:p.Ala297=
NM_001271100.2:c.797C= NP_001258029.1:p.Ala266=
NM_001362895.2:c.1088C= NP_001349824.1:p.Ala363=
NM_001362896.2:c.1088C= NP_001349825.1:p.Ala363=
NM_001362897.2:c.1037C= NP_001349826.1:p.Ala346=
NM_014281.5:c.926C= NP_055096.2:p.Ala309=
NM_078480.3:c.977C= MANE Select NP_510965.1:p.Ala326=