Canonical Allele Identifier: CA2340593076
Gene: FUZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49807569_49807575delinsCCCTCTT , CM000681.2:g.49807569_49807575delinsCCCTCTT GRCh38
NC_000019.9:g.50310826_50310832delinsCCCTCTT , CM000681.1:g.50310826_50310832delinsCCCTCTT GRCh37
NC_000019.8:g.55002638_55002644delinsCCCTCTT NCBI36
NG_032843.1:g.10736_10742delinsAAGAGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000313777.9:c.1034-201_1034-195delinsAAGAGGG MANE Select ENSP00000313309.4:n.1034-201_1034-195delinsAAGAGGG
ENST00000313777.8:c.1034-201_1034-195delinsAAGAGGG ENSP00000313309.4:n.1034-201_1034-195delinsAAGAGGG
ENST00000377092.8:c.*774-201_*774-195delinsAAGAGGG ENSP00000366296.5:n.*774-201_*774-195delinsAAGAGGG
ENST00000525130.5:c.*688-201_*688-195delinsAAGAGGG ENSP00000433492.1:n.*688-201_*688-195delinsAAGAGGG
ENST00000525370.5:c.*691-201_*691-195delinsAAGAGGG ENSP00000431420.1:n.*691-201_*691-195delinsAAGAGGG
ENST00000528094.5:c.926-201_926-195delinsAAGAGGG ENSP00000435177.1:n.926-201_926-195delinsAAGAGGG
ENST00000529634.2:c.190-201_190-195delinsAAGAGGG
ENST00000533418.5:c.884-201_884-195delinsAAGAGGG ENSP00000431731.1:n.884-201_884-195delinsAAGAGGG
NM_001171937.1:c.926-201_926-195delinsAAGAGGG NP_001165408.1:n.926-201_926-195delinsAAGAGGG
NM_025129.4:c.1034-201_1034-195delinsAAGAGGG NP_079405.2:n.1034-201_1034-195delinsAAGAGGG
NR_033269.1:n.1153-201_1153-195delinsAAGAGGG
XM_006723399.2:c.*20-201_*20-195delinsAAGAGGG XP_006723462.1:n.*20-201_*20-195delinsAAGAGGG
XM_011527339.1:c.1037-201_1037-195delinsAAGAGGG XP_011525641.1:n.1037-201_1037-195delinsAAGAGGG
XM_011527340.1:c.887-201_887-195delinsAAGAGGG XP_011525642.1:n.887-201_887-195delinsAAGAGGG
XM_011527341.1:c.887-201_887-195delinsAAGAGGG XP_011525643.1:n.887-201_887-195delinsAAGAGGG
XM_011527342.1:c.866-201_866-195delinsAAGAGGG XP_011525644.1:n.866-201_866-195delinsAAGAGGG
XM_011527343.1:c.*20-201_*20-195delinsAAGAGGG XP_011525645.1:n.*20-201_*20-195delinsAAGAGGG
XM_011527344.1:c.839-201_839-195delinsAAGAGGG XP_011525646.1:n.839-201_839-195delinsAAGAGGG
XM_011527345.1:c.737-201_737-195delinsAAGAGGG XP_011525647.1:n.737-201_737-195delinsAAGAGGG
XM_011527346.1:c.737-201_737-195delinsAAGAGGG XP_011525648.1:n.737-201_737-195delinsAAGAGGG
XM_011527347.1:c.737-201_737-195delinsAAGAGGG XP_011525649.1:n.737-201_737-195delinsAAGAGGG
XR_935862.1:n.1396_1401+1delinsAAGAGGG
NM_001352262.1:c.1037-201_1037-195delinsAAGAGGG NP_001339191.1:n.1037-201_1037-195delinsAAGAGGG
NM_001363663.1:c.884-201_884-195delinsAAGAGGG NP_001350592.1:n.884-201_884-195delinsAAGAGGG
XM_006723399.3:c.*20-201_*20-195delinsAAGAGGG XP_006723462.1:n.*20-201_*20-195delinsAAGAGGG
XM_011527341.2:c.887-201_887-195delinsAAGAGGG XP_011525643.1:n.887-201_887-195delinsAAGAGGG
XM_011527342.2:c.866-201_866-195delinsAAGAGGG XP_011525644.1:n.866-201_866-195delinsAAGAGGG
XM_017027320.1:c.*20-180_*20-174delinsAAGAGGG XP_016882809.1:n.*20-180_*20-174delinsAAGAGGG
XM_017027321.1:c.734-201_734-195delinsAAGAGGG XP_016882810.1:n.734-201_734-195delinsAAGAGGG
XM_017027322.2:c.*20-201_*20-195delinsAAGAGGG XP_016882811.1:n.*20-201_*20-195delinsAAGAGGG
XM_024451729.1:c.866-201_866-195delinsAAGAGGG XP_024307497.1:n.866-201_866-195delinsAAGAGGG
XM_024451730.1:c.863-201_863-195delinsAAGAGGG XP_024307498.1:n.863-201_863-195delinsAAGAGGG
XR_001753764.1:n.1803_1808+1delinsAAGAGGG
XR_001753765.1:n.1109-201_1109-195delinsAAGAGGG
XR_002958363.1:n.2054_2059+1delinsAAGAGGG
XR_002958364.1:n.1800_1805+1delinsAAGAGGG
XR_002958365.1:n.1693_1698+1delinsAAGAGGG
NM_001171937.2:c.926-201_926-195delinsAAGAGGG NP_001165408.1:n.926-201_926-195delinsAAGAGGG
NM_001352262.2:c.1037-201_1037-195delinsAAGAGGG NP_001339191.1:n.1037-201_1037-195delinsAAGAGGG
NM_025129.5:c.1034-201_1034-195delinsAAGAGGG MANE Select NP_079405.2:n.1034-201_1034-195delinsAAGAGGG
NR_033269.2:n.1135-201_1135-195delinsAAGAGGG