Canonical Allele Identifier: CA2340592960
Gene: FUZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49807326A= , CM000681.2:g.49807326A= GRCh38
NC_000019.9:g.50310583A= , CM000681.1:g.50310583A= GRCh37
NC_000019.8:g.55002395A= NCBI36
NG_032843.1:g.10985T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313777.9:c.1082T= MANE Select ENSP00000313309.4:p.Leu361=
ENST00000313777.8:c.1082T= ENSP00000313309.4:p.Leu361=
ENST00000377092.8:c.*822T= ENSP00000366296.5:n.*822T=
ENST00000525130.5:c.*736T= ENSP00000433492.1:n.*736T=
ENST00000525370.5:c.*739T= ENSP00000431420.1:n.*739T=
ENST00000528094.5:c.974T= ENSP00000435177.1:p.Leu325=
ENST00000529634.2:c.238T=
ENST00000533418.5:c.932T= ENSP00000431731.1:p.Leu311=
NM_001171937.1:c.974T= NP_001165408.1:p.Leu325=
NM_025129.4:c.1082T= NP_079405.2:p.Leu361=
NR_033269.1:n.1201T=
XM_006723399.2:c.*68T= XP_006723462.1:n.*68T=
XM_011527339.1:c.1085T= XP_011525641.1:p.Leu362=
XM_011527340.1:c.935T= XP_011525642.1:p.Leu312=
XM_011527341.1:c.935T= XP_011525643.1:p.Leu312=
XM_011527342.1:c.914T= XP_011525644.1:p.Leu305=
XM_011527343.1:c.*68T= XP_011525645.1:n.*68T=
XM_011527344.1:c.887T= XP_011525646.1:p.Leu296=
XM_011527345.1:c.785T= XP_011525647.1:p.Leu262=
XM_011527346.1:c.785T= XP_011525648.1:p.Leu262=
XM_011527347.1:c.785T= XP_011525649.1:p.Leu262=
XR_935862.1:n.1450T=
NM_001352262.1:c.1085T= NP_001339191.1:p.Leu362=
NM_001363663.1:c.932T= NP_001350592.1:p.Leu311=
XM_006723399.3:c.*68T= XP_006723462.1:n.*68T=
XM_011527341.2:c.935T= XP_011525643.1:p.Leu312=
XM_011527342.2:c.914T= XP_011525644.1:p.Leu305=
XM_017027321.1:c.782T= XP_016882810.1:p.Leu261=
XM_017027322.2:c.*68T= XP_016882811.1:n.*68T=
XM_024451729.1:c.914T= XP_024307497.1:p.Leu305=
XM_024451730.1:c.911T= XP_024307498.1:p.Leu304=
XR_001753764.1:n.1857T=
XR_001753765.1:n.1157T=
XR_002958363.1:n.2108T=
XR_002958364.1:n.1854T=
XR_002958365.1:n.1747T=
NM_001171937.2:c.974T= NP_001165408.1:p.Leu325=
NM_001352262.2:c.1085T= NP_001339191.1:p.Leu362=
NM_025129.5:c.1082T= MANE Select NP_079405.2:p.Leu361=
NR_033269.2:n.1183T=