Canonical Allele Identifier: CA2340592969
Gene: FUZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49807349T= , CM000681.2:g.49807349T= GRCh38
NC_000019.9:g.50310606T= , CM000681.1:g.50310606T= GRCh37
NC_000019.8:g.55002418T= NCBI36
NG_032843.1:g.10962A=

Transcript Alleles

HGVS Amino-acid change
ENST00000313777.9:c.1059A= MANE Select ENSP00000313309.4:p.Glu353=
ENST00000313777.8:c.1059A= ENSP00000313309.4:p.Glu353=
ENST00000377092.8:c.*799A= ENSP00000366296.5:n.*799A=
ENST00000525130.5:c.*713A= ENSP00000433492.1:n.*713A=
ENST00000525370.5:c.*716A= ENSP00000431420.1:n.*716A=
ENST00000528094.5:c.951A= ENSP00000435177.1:p.Glu317=
ENST00000529634.2:c.215A=
ENST00000533418.5:c.909A= ENSP00000431731.1:p.Glu303=
NM_001171937.1:c.951A= NP_001165408.1:p.Glu317=
NM_025129.4:c.1059A= NP_079405.2:p.Glu353=
NR_033269.1:n.1178A=
XM_006723399.2:c.*45A= XP_006723462.1:n.*45A=
XM_011527339.1:c.1062A= XP_011525641.1:p.Glu354=
XM_011527340.1:c.912A= XP_011525642.1:p.Glu304=
XM_011527341.1:c.912A= XP_011525643.1:p.Glu304=
XM_011527342.1:c.891A= XP_011525644.1:p.Glu297=
XM_011527343.1:c.*45A= XP_011525645.1:n.*45A=
XM_011527344.1:c.864A= XP_011525646.1:p.Glu288=
XM_011527345.1:c.762A= XP_011525647.1:p.Glu254=
XM_011527346.1:c.762A= XP_011525648.1:p.Glu254=
XM_011527347.1:c.762A= XP_011525649.1:p.Glu254=
XR_935862.1:n.1427A=
NM_001352262.1:c.1062A= NP_001339191.1:p.Glu354=
NM_001363663.1:c.909A= NP_001350592.1:p.Glu303=
XM_006723399.3:c.*45A= XP_006723462.1:n.*45A=
XM_011527341.2:c.912A= XP_011525643.1:p.Glu304=
XM_011527342.2:c.891A= XP_011525644.1:p.Glu297=
XM_017027321.1:c.759A= XP_016882810.1:p.Glu253=
XM_017027322.2:c.*45A= XP_016882811.1:n.*45A=
XM_024451729.1:c.891A= XP_024307497.1:p.Glu297=
XM_024451730.1:c.888A= XP_024307498.1:p.Glu296=
XR_001753764.1:n.1834A=
XR_001753765.1:n.1134A=
XR_002958363.1:n.2085A=
XR_002958364.1:n.1831A=
XR_002958365.1:n.1724A=
NM_001171937.2:c.951A= NP_001165408.1:p.Glu317=
NM_001352262.2:c.1062A= NP_001339191.1:p.Glu354=
NM_025129.5:c.1059A= MANE Select NP_079405.2:p.Glu353=
NR_033269.2:n.1160A=