Canonical Allele Identifier: CA2814700700

Gene: FUZ

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49807526G>A , CM000681.2:g.49807526G>A	GRCh38
NC_000019.9:g.50310783G>A , CM000681.1:g.50310783G>A	GRCh37
NC_000019.8:g.55002595G>A	NCBI36
NG_032843.1:g.10785C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313777.9:c.1034-152C>T MANE Select	ENSP00000313309.4:n.1034-152C>T
ENST00000313777.8:c.1034-152C>T	ENSP00000313309.4:n.1034-152C>T
ENST00000377092.8:c.*774-152C>T	ENSP00000366296.5:n.*774-152C>T
ENST00000525130.5:c.*688-152C>T	ENSP00000433492.1:n.*688-152C>T
ENST00000525370.5:c.*691-152C>T	ENSP00000431420.1:n.*691-152C>T
ENST00000528094.5:c.926-152C>T	ENSP00000435177.1:n.926-152C>T
ENST00000529634.2:c.190-152C>T
ENST00000533418.5:c.884-152C>T	ENSP00000431731.1:n.884-152C>T
NM_001171937.1:c.926-152C>T	NP_001165408.1:n.926-152C>T
NM_025129.4:c.1034-152C>T	NP_079405.2:n.1034-152C>T
NR_033269.1:n.1153-152C>T
XM_006723399.2:c.*20-152C>T	XP_006723462.1:n.*20-152C>T
XM_011527339.1:c.1037-152C>T	XP_011525641.1:n.1037-152C>T
XM_011527340.1:c.887-152C>T	XP_011525642.1:n.887-152C>T
XM_011527341.1:c.887-152C>T	XP_011525643.1:n.887-152C>T
XM_011527342.1:c.866-152C>T	XP_011525644.1:n.866-152C>T
XM_011527343.1:c.*20-152C>T	XP_011525645.1:n.*20-152C>T
XM_011527344.1:c.839-152C>T	XP_011525646.1:n.839-152C>T
XM_011527345.1:c.737-152C>T	XP_011525647.1:n.737-152C>T
XM_011527346.1:c.737-152C>T	XP_011525648.1:n.737-152C>T
XM_011527347.1:c.737-152C>T	XP_011525649.1:n.737-152C>T
XR_935862.1:n.1401+44C>T
NM_001352262.1:c.1037-152C>T	NP_001339191.1:n.1037-152C>T
NM_001363663.1:c.884-152C>T	NP_001350592.1:n.884-152C>T
XM_006723399.3:c.*20-152C>T	XP_006723462.1:n.*20-152C>T
XM_011527341.2:c.887-152C>T	XP_011525643.1:n.887-152C>T
XM_011527342.2:c.866-152C>T	XP_011525644.1:n.866-152C>T
XM_017027320.1:c.*20-131C>T	XP_016882809.1:n.*20-131C>T
XM_017027321.1:c.734-152C>T	XP_016882810.1:n.734-152C>T
XM_017027322.2:c.*20-152C>T	XP_016882811.1:n.*20-152C>T
XM_024451729.1:c.866-152C>T	XP_024307497.1:n.866-152C>T
XM_024451730.1:c.863-152C>T	XP_024307498.1:n.863-152C>T
XR_001753764.1:n.1808+44C>T
XR_001753765.1:n.1109-152C>T
XR_002958363.1:n.2059+44C>T
XR_002958364.1:n.1805+44C>T
XR_002958365.1:n.1698+44C>T
NM_001171937.2:c.926-152C>T	NP_001165408.1:n.926-152C>T
NM_001352262.2:c.1037-152C>T	NP_001339191.1:n.1037-152C>T
NM_025129.5:c.1034-152C>T MANE Select	NP_079405.2:n.1034-152C>T
NR_033269.2:n.1135-152C>T