Canonical Allele Identifier: CA2340592968
Gene: FUZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49807348C= , CM000681.2:g.49807348C= GRCh38
NC_000019.9:g.50310605C= , CM000681.1:g.50310605C= GRCh37
NC_000019.8:g.55002417C= NCBI36
NG_032843.1:g.10963G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313777.9:c.1060G= MANE Select ENSP00000313309.4:p.Asp354=
ENST00000313777.8:c.1060G= ENSP00000313309.4:p.Asp354=
ENST00000377092.8:c.*800G= ENSP00000366296.5:n.*800G=
ENST00000525130.5:c.*714G= ENSP00000433492.1:n.*714G=
ENST00000525370.5:c.*717G= ENSP00000431420.1:n.*717G=
ENST00000528094.5:c.952G= ENSP00000435177.1:p.Asp318=
ENST00000529634.2:c.216G=
ENST00000533418.5:c.910G= ENSP00000431731.1:p.Asp304=
NM_001171937.1:c.952G= NP_001165408.1:p.Asp318=
NM_025129.4:c.1060G= NP_079405.2:p.Asp354=
NR_033269.1:n.1179G=
XM_006723399.2:c.*46G= XP_006723462.1:n.*46G=
XM_011527339.1:c.1063G= XP_011525641.1:p.Asp355=
XM_011527340.1:c.913G= XP_011525642.1:p.Asp305=
XM_011527341.1:c.913G= XP_011525643.1:p.Asp305=
XM_011527342.1:c.892G= XP_011525644.1:p.Asp298=
XM_011527343.1:c.*46G= XP_011525645.1:n.*46G=
XM_011527344.1:c.865G= XP_011525646.1:p.Asp289=
XM_011527345.1:c.763G= XP_011525647.1:p.Asp255=
XM_011527346.1:c.763G= XP_011525648.1:p.Asp255=
XM_011527347.1:c.763G= XP_011525649.1:p.Asp255=
XR_935862.1:n.1428G=
NM_001352262.1:c.1063G= NP_001339191.1:p.Asp355=
NM_001363663.1:c.910G= NP_001350592.1:p.Asp304=
XM_006723399.3:c.*46G= XP_006723462.1:n.*46G=
XM_011527341.2:c.913G= XP_011525643.1:p.Asp305=
XM_011527342.2:c.892G= XP_011525644.1:p.Asp298=
XM_017027321.1:c.760G= XP_016882810.1:p.Asp254=
XM_017027322.2:c.*46G= XP_016882811.1:n.*46G=
XM_024451729.1:c.892G= XP_024307497.1:p.Asp298=
XM_024451730.1:c.889G= XP_024307498.1:p.Asp297=
XR_001753764.1:n.1835G=
XR_001753765.1:n.1135G=
XR_002958363.1:n.2086G=
XR_002958364.1:n.1832G=
XR_002958365.1:n.1725G=
NM_001171937.2:c.952G= NP_001165408.1:p.Asp318=
NM_001352262.2:c.1063G= NP_001339191.1:p.Asp355=
NM_025129.5:c.1060G= MANE Select NP_079405.2:p.Asp354=
NR_033269.2:n.1161G=