Canonical Allele Identifier: CA406900105

Gene: FUZ

Linked Data

• MyVariant Identifiers: chr19:g.50310518A>C (hg19) ; chr19:g.49807261A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49807261A>C , CM000681.2:g.49807261A>C	GRCh38
NC_000019.9:g.50310518A>C , CM000681.1:g.50310518A>C	GRCh37
NC_000019.8:g.55002330A>C	NCBI36
NG_032843.1:g.11050T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000313777.9:c.1147T>G MANE Select	ENSP00000313309.4:p.Leu383Val
ENST00000313777.8:c.1147T>G	ENSP00000313309.4:p.Leu383Val
ENST00000377092.8:c.*887T>G	ENSP00000366296.5:n.*887T>G
ENST00000525130.5:c.*801T>G	ENSP00000433492.1:n.*801T>G
ENST00000525370.5:c.*804T>G	ENSP00000431420.1:n.*804T>G
ENST00000528094.5:c.1039T>G	ENSP00000435177.1:p.Leu347Val
ENST00000529634.2:c.303T>G
ENST00000533418.5:c.997T>G	ENSP00000431731.1:p.Leu333Val
NM_001171937.1:c.1039T>G	NP_001165408.1:p.Leu347Val
NM_025129.4:c.1147T>G	NP_079405.2:p.Leu383Val
NR_033269.1:n.1266T>G
XM_006723399.2:c.*133T>G	XP_006723462.1:n.*133T>G
XM_011527339.1:c.1150T>G	XP_011525641.1:p.Leu384Val
XM_011527340.1:c.1000T>G	XP_011525642.1:p.Leu334Val
XM_011527341.1:c.1000T>G	XP_011525643.1:p.Leu334Val
XM_011527342.1:c.979T>G	XP_011525644.1:p.Leu327Val
XM_011527343.1:c.*133T>G	XP_011525645.1:n.*133T>G
XM_011527344.1:c.952T>G	XP_011525646.1:p.Leu318Val
XM_011527345.1:c.850T>G	XP_011525647.1:p.Leu284Val
XM_011527346.1:c.850T>G	XP_011525648.1:p.Leu284Val
XM_011527347.1:c.850T>G	XP_011525649.1:p.Leu284Val
NM_001352262.1:c.1150T>G	NP_001339191.1:p.Leu384Val
NM_001363663.1:c.997T>G	NP_001350592.1:p.Leu333Val
XM_006723399.3:c.*133T>G	XP_006723462.1:n.*133T>G
XM_011527341.2:c.1000T>G	XP_011525643.1:p.Leu334Val
XM_011527342.2:c.979T>G	XP_011525644.1:p.Leu327Val
XM_017027321.1:c.847T>G	XP_016882810.1:p.Leu283Val
XM_017027322.2:c.*133T>G	XP_016882811.1:n.*133T>G
XM_024451729.1:c.979T>G	XP_024307497.1:p.Leu327Val
XM_024451730.1:c.976T>G	XP_024307498.1:p.Leu326Val
XR_001753764.1:n.1922T>G
XR_001753765.1:n.1222T>G
XR_002958363.1:n.2173T>G
XR_002958364.1:n.1919T>G
XR_002958365.1:n.1812T>G
NM_001171937.2:c.1039T>G	NP_001165408.1:p.Leu347Val
NM_001352262.2:c.1150T>G	NP_001339191.1:p.Leu384Val
NM_025129.5:c.1147T>G MANE Select	NP_079405.2:p.Leu383Val
NR_033269.2:n.1248T>G