Canonical Allele Identifier: CA406900060

Gene: FUZ

Linked Data

• MyVariant Identifiers: chr19:g.50310508C>T (hg19) ; chr19:g.49807251C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49807251C>T , CM000681.2:g.49807251C>T	GRCh38
NC_000019.9:g.50310508C>T , CM000681.1:g.50310508C>T	GRCh37
NC_000019.8:g.55002320C>T	NCBI36
NG_032843.1:g.11060G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000313777.9:c.1157G>A MANE Select	ENSP00000313309.4:p.Gly386Glu
ENST00000313777.8:c.1157G>A	ENSP00000313309.4:p.Gly386Glu
ENST00000377092.8:c.*897G>A	ENSP00000366296.5:n.*897G>A
ENST00000525130.5:c.*811G>A	ENSP00000433492.1:n.*811G>A
ENST00000525370.5:c.*814G>A	ENSP00000431420.1:n.*814G>A
ENST00000528094.5:c.1049G>A	ENSP00000435177.1:p.Gly350Glu
ENST00000529634.2:c.313G>A
ENST00000533418.5:c.1007G>A	ENSP00000431731.1:p.Gly336Glu
NM_001171937.1:c.1049G>A	NP_001165408.1:p.Gly350Glu
NM_025129.4:c.1157G>A	NP_079405.2:p.Gly386Glu
NR_033269.1:n.1276G>A
XM_006723399.2:c.*143G>A	XP_006723462.1:n.*143G>A
XM_011527339.1:c.1160G>A	XP_011525641.1:p.Gly387Glu
XM_011527340.1:c.1010G>A	XP_011525642.1:p.Gly337Glu
XM_011527341.1:c.1010G>A	XP_011525643.1:p.Gly337Glu
XM_011527342.1:c.989G>A	XP_011525644.1:p.Gly330Glu
XM_011527343.1:c.*143G>A	XP_011525645.1:n.*143G>A
XM_011527344.1:c.962G>A	XP_011525646.1:p.Gly321Glu
XM_011527345.1:c.860G>A	XP_011525647.1:p.Gly287Glu
XM_011527346.1:c.860G>A	XP_011525648.1:p.Gly287Glu
XM_011527347.1:c.860G>A	XP_011525649.1:p.Gly287Glu
NM_001352262.1:c.1160G>A	NP_001339191.1:p.Gly387Glu
NM_001363663.1:c.1007G>A	NP_001350592.1:p.Gly336Glu
XM_006723399.3:c.*143G>A	XP_006723462.1:n.*143G>A
XM_011527341.2:c.1010G>A	XP_011525643.1:p.Gly337Glu
XM_011527342.2:c.989G>A	XP_011525644.1:p.Gly330Glu
XM_017027321.1:c.857G>A	XP_016882810.1:p.Gly286Glu
XM_017027322.2:c.*143G>A	XP_016882811.1:n.*143G>A
XM_024451729.1:c.989G>A	XP_024307497.1:p.Gly330Glu
XM_024451730.1:c.986G>A	XP_024307498.1:p.Gly329Glu
XR_001753764.1:n.1932G>A
XR_001753765.1:n.1232G>A
XR_002958363.1:n.2183G>A
XR_002958364.1:n.1929G>A
XR_002958365.1:n.1822G>A
NM_001171937.2:c.1049G>A	NP_001165408.1:p.Gly350Glu
NM_001352262.2:c.1160G>A	NP_001339191.1:p.Gly387Glu
NM_025129.5:c.1157G>A MANE Select	NP_079405.2:p.Gly386Glu
NR_033269.2:n.1258G>A