Canonical Allele Identifier: CA2340592946
Gene: FUZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49807287G= , CM000681.2:g.49807287G= GRCh38
NC_000019.9:g.50310544G= , CM000681.1:g.50310544G= GRCh37
NC_000019.8:g.55002356G= NCBI36
NG_032843.1:g.11024C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313777.9:c.1121C= MANE Select ENSP00000313309.4:p.Pro374=
ENST00000313777.8:c.1121C= ENSP00000313309.4:p.Pro374=
ENST00000377092.8:c.*861C= ENSP00000366296.5:n.*861C=
ENST00000525130.5:c.*775C= ENSP00000433492.1:n.*775C=
ENST00000525370.5:c.*778C= ENSP00000431420.1:n.*778C=
ENST00000528094.5:c.1013C= ENSP00000435177.1:p.Pro338=
ENST00000529634.2:c.277C=
ENST00000533418.5:c.971C= ENSP00000431731.1:p.Pro324=
NM_001171937.1:c.1013C= NP_001165408.1:p.Pro338=
NM_025129.4:c.1121C= NP_079405.2:p.Pro374=
NR_033269.1:n.1240C=
XM_006723399.2:c.*107C= XP_006723462.1:n.*107C=
XM_011527339.1:c.1124C= XP_011525641.1:p.Pro375=
XM_011527340.1:c.974C= XP_011525642.1:p.Pro325=
XM_011527341.1:c.974C= XP_011525643.1:p.Pro325=
XM_011527342.1:c.953C= XP_011525644.1:p.Pro318=
XM_011527343.1:c.*107C= XP_011525645.1:n.*107C=
XM_011527344.1:c.926C= XP_011525646.1:p.Pro309=
XM_011527345.1:c.824C= XP_011525647.1:p.Pro275=
XM_011527346.1:c.824C= XP_011525648.1:p.Pro275=
XM_011527347.1:c.824C= XP_011525649.1:p.Pro275=
XR_935862.1:n.1489C=
NM_001352262.1:c.1124C= NP_001339191.1:p.Pro375=
NM_001363663.1:c.971C= NP_001350592.1:p.Pro324=
XM_006723399.3:c.*107C= XP_006723462.1:n.*107C=
XM_011527341.2:c.974C= XP_011525643.1:p.Pro325=
XM_011527342.2:c.953C= XP_011525644.1:p.Pro318=
XM_017027321.1:c.821C= XP_016882810.1:p.Pro274=
XM_017027322.2:c.*107C= XP_016882811.1:n.*107C=
XM_024451729.1:c.953C= XP_024307497.1:p.Pro318=
XM_024451730.1:c.950C= XP_024307498.1:p.Pro317=
XR_001753764.1:n.1896C=
XR_001753765.1:n.1196C=
XR_002958363.1:n.2147C=
XR_002958364.1:n.1893C=
XR_002958365.1:n.1786C=
NM_001171937.2:c.1013C= NP_001165408.1:p.Pro338=
NM_001352262.2:c.1124C= NP_001339191.1:p.Pro375=
NM_025129.5:c.1121C= MANE Select NP_079405.2:p.Pro374=
NR_033269.2:n.1222C=