Canonical Allele Identifier: CA2340593002

Gene: FUZ

Linked Data

• dbSNP Id: rs2073442880
• gnomAD v4: 19-49807411-GCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49807412_49807413del , CM000681.2:g.49807412_49807413del	GRCh38
NC_000019.9:g.50310669_50310670del , CM000681.1:g.50310669_50310670del	GRCh37
NC_000019.8:g.55002481_55002482del	NCBI36
NG_032843.1:g.10898_10899del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313777.9:c.1034-39_1034-38del MANE Select	ENSP00000313309.4:n.1034-39_1034-38del
ENST00000313777.8:c.1034-39_1034-38del	ENSP00000313309.4:n.1034-39_1034-38del
ENST00000377092.8:c.*774-39_*774-38del	ENSP00000366296.5:n.*774-39_*774-38del
ENST00000525130.5:c.*688-39_*688-38del	ENSP00000433492.1:n.*688-39_*688-38del
ENST00000525370.5:c.*691-39_*691-38del	ENSP00000431420.1:n.*691-39_*691-38del
ENST00000528094.5:c.926-39_926-38del	ENSP00000435177.1:n.926-39_926-38del
ENST00000529634.2:c.190-39_190-38del
ENST00000533418.5:c.884-39_884-38del	ENSP00000431731.1:n.884-39_884-38del
NM_001171937.1:c.926-39_926-38del	NP_001165408.1:n.926-39_926-38del
NM_025129.4:c.1034-39_1034-38del	NP_079405.2:n.1034-39_1034-38del
NR_033269.1:n.1153-39_1153-38del
XM_006723399.2:c.*20-39_*20-38del	XP_006723462.1:n.*20-39_*20-38del
XM_011527339.1:c.1037-39_1037-38del	XP_011525641.1:n.1037-39_1037-38del
XM_011527340.1:c.887-39_887-38del	XP_011525642.1:n.887-39_887-38del
XM_011527341.1:c.887-39_887-38del	XP_011525643.1:n.887-39_887-38del
XM_011527342.1:c.866-39_866-38del	XP_011525644.1:n.866-39_866-38del
XM_011527343.1:c.*20-39_*20-38del	XP_011525645.1:n.*20-39_*20-38del
XM_011527344.1:c.839-39_839-38del	XP_011525646.1:n.839-39_839-38del
XM_011527345.1:c.737-39_737-38del	XP_011525647.1:n.737-39_737-38del
XM_011527346.1:c.737-39_737-38del	XP_011525648.1:n.737-39_737-38del
XM_011527347.1:c.737-39_737-38del	XP_011525649.1:n.737-39_737-38del
XR_935862.1:n.1402-39_1402-38del
NM_001352262.1:c.1037-39_1037-38del	NP_001339191.1:n.1037-39_1037-38del
NM_001363663.1:c.884-39_884-38del	NP_001350592.1:n.884-39_884-38del
XM_006723399.3:c.*20-39_*20-38del	XP_006723462.1:n.*20-39_*20-38del
XM_011527341.2:c.887-39_887-38del	XP_011525643.1:n.887-39_887-38del
XM_011527342.2:c.866-39_866-38del	XP_011525644.1:n.866-39_866-38del
XM_017027320.1:c.*20-18_*20-17del	XP_016882809.1:n.*20-18_*20-17del
XM_017027321.1:c.734-39_734-38del	XP_016882810.1:n.734-39_734-38del
XM_017027322.2:c.*20-39_*20-38del	XP_016882811.1:n.*20-39_*20-38del
XM_024451729.1:c.866-39_866-38del	XP_024307497.1:n.866-39_866-38del
XM_024451730.1:c.863-39_863-38del	XP_024307498.1:n.863-39_863-38del
XR_001753764.1:n.1809-39_1809-38del
XR_001753765.1:n.1109-39_1109-38del
XR_002958363.1:n.2060-39_2060-38del
XR_002958364.1:n.1806-39_1806-38del
XR_002958365.1:n.1699-39_1699-38del
NM_001171937.2:c.926-39_926-38del	NP_001165408.1:n.926-39_926-38del
NM_001352262.2:c.1037-39_1037-38del	NP_001339191.1:n.1037-39_1037-38del
NM_025129.5:c.1034-39_1034-38del MANE Select	NP_079405.2:n.1034-39_1034-38del
NR_033269.2:n.1135-39_1135-38del