Canonical Allele Identifier: CA406900481
Gene: FUZ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49807357T>A , CM000681.2:g.49807357T>A GRCh38
NC_000019.9:g.50310614T>A , CM000681.1:g.50310614T>A GRCh37
NC_000019.8:g.55002426T>A NCBI36
NG_032843.1:g.10954A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000313777.9:c.1051A>T MANE Select ENSP00000313309.4:p.Lys351Ter
ENST00000313777.8:c.1051A>T ENSP00000313309.4:p.Lys351Ter
ENST00000377092.8:c.*791A>T ENSP00000366296.5:n.*791A>T
ENST00000525130.5:c.*705A>T ENSP00000433492.1:n.*705A>T
ENST00000525370.5:c.*708A>T ENSP00000431420.1:n.*708A>T
ENST00000528094.5:c.943A>T ENSP00000435177.1:p.Lys315Ter
ENST00000529634.2:c.207A>T
ENST00000533418.5:c.901A>T ENSP00000431731.1:p.Lys301Ter
NM_001171937.1:c.943A>T NP_001165408.1:p.Lys315Ter
NM_025129.4:c.1051A>T NP_079405.2:p.Lys351Ter
NR_033269.1:n.1170A>T
XM_006723399.2:c.*37A>T XP_006723462.1:n.*37A>T
XM_011527339.1:c.1054A>T XP_011525641.1:p.Lys352Ter
XM_011527340.1:c.904A>T XP_011525642.1:p.Lys302Ter
XM_011527341.1:c.904A>T XP_011525643.1:p.Lys302Ter
XM_011527342.1:c.883A>T XP_011525644.1:p.Lys295Ter
XM_011527343.1:c.*37A>T XP_011525645.1:n.*37A>T
XM_011527344.1:c.856A>T XP_011525646.1:p.Lys286Ter
XM_011527345.1:c.754A>T XP_011525647.1:p.Lys252Ter
XM_011527346.1:c.754A>T XP_011525648.1:p.Lys252Ter
XM_011527347.1:c.754A>T XP_011525649.1:p.Lys252Ter
XR_935862.1:n.1419A>T
NM_001352262.1:c.1054A>T NP_001339191.1:p.Lys352Ter
NM_001363663.1:c.901A>T NP_001350592.1:p.Lys301Ter
XM_006723399.3:c.*37A>T XP_006723462.1:n.*37A>T
XM_011527341.2:c.904A>T XP_011525643.1:p.Lys302Ter
XM_011527342.2:c.883A>T XP_011525644.1:p.Lys295Ter
XM_017027321.1:c.751A>T XP_016882810.1:p.Lys251Ter
XM_017027322.2:c.*37A>T XP_016882811.1:n.*37A>T
XM_024451729.1:c.883A>T XP_024307497.1:p.Lys295Ter
XM_024451730.1:c.880A>T XP_024307498.1:p.Lys294Ter
XR_001753764.1:n.1826A>T
XR_001753765.1:n.1126A>T
XR_002958363.1:n.2077A>T
XR_002958364.1:n.1823A>T
XR_002958365.1:n.1716A>T
NM_001171937.2:c.943A>T NP_001165408.1:p.Lys315Ter
NM_001352262.2:c.1054A>T NP_001339191.1:p.Lys352Ter
NM_025129.5:c.1051A>T MANE Select NP_079405.2:p.Lys351Ter
NR_033269.2:n.1152A>T