Canonical Allele Identifier: CA406899870

Gene: FUZ

Linked Data

• MyVariant Identifiers: chr19:g.50310455G>C (hg19) ; chr19:g.49807198G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49807198G>C , CM000681.2:g.49807198G>C	GRCh38
NC_000019.9:g.50310455G>C , CM000681.1:g.50310455G>C	GRCh37
NC_000019.8:g.55002267G>C	NCBI36
NG_032843.1:g.11113C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313777.9:c.1210C>G MANE Select	ENSP00000313309.4:p.Arg404Gly
ENST00000313777.8:c.1210C>G	ENSP00000313309.4:p.Arg404Gly
ENST00000377092.8:c.*950C>G	ENSP00000366296.5:n.*950C>G
ENST00000525130.5:c.*864C>G	ENSP00000433492.1:n.*864C>G
ENST00000525370.5:c.*867C>G	ENSP00000431420.1:n.*867C>G
ENST00000528094.5:c.1102C>G	ENSP00000435177.1:p.Arg368Gly
ENST00000529634.2:c.366C>G
ENST00000533418.5:c.1060C>G	ENSP00000431731.1:p.Arg354Gly
NM_001171937.1:c.1102C>G	NP_001165408.1:p.Arg368Gly
NM_025129.4:c.1210C>G	NP_079405.2:p.Arg404Gly
NR_033269.1:n.1329C>G
XM_006723399.2:c.*196C>G	XP_006723462.1:n.*196C>G
XM_011527339.1:c.1213C>G	XP_011525641.1:p.Arg405Gly
XM_011527340.1:c.1063C>G	XP_011525642.1:p.Arg355Gly
XM_011527341.1:c.1063C>G	XP_011525643.1:p.Arg355Gly
XM_011527342.1:c.1042C>G	XP_011525644.1:p.Arg348Gly
XM_011527343.1:c.*196C>G	XP_011525645.1:n.*196C>G
XM_011527344.1:c.1015C>G	XP_011525646.1:p.Arg339Gly
XM_011527345.1:c.913C>G	XP_011525647.1:p.Arg305Gly
XM_011527346.1:c.913C>G	XP_011525648.1:p.Arg305Gly
XM_011527347.1:c.913C>G	XP_011525649.1:p.Arg305Gly
NM_001352262.1:c.1213C>G	NP_001339191.1:p.Arg405Gly
NM_001363663.1:c.1060C>G	NP_001350592.1:p.Arg354Gly
XM_006723399.3:c.*196C>G	XP_006723462.1:n.*196C>G
XM_011527341.2:c.1063C>G	XP_011525643.1:p.Arg355Gly
XM_011527342.2:c.1042C>G	XP_011525644.1:p.Arg348Gly
XM_017027321.1:c.910C>G	XP_016882810.1:p.Arg304Gly
XM_017027322.2:c.*196C>G	XP_016882811.1:n.*196C>G
XM_024451729.1:c.1042C>G	XP_024307497.1:p.Arg348Gly
XM_024451730.1:c.1039C>G	XP_024307498.1:p.Arg347Gly
XR_001753764.1:n.1985C>G
XR_001753765.1:n.1285C>G
XR_002958363.1:n.2236C>G
XR_002958364.1:n.1982C>G
XR_002958365.1:n.1875C>G
NM_001171937.2:c.1102C>G	NP_001165408.1:p.Arg368Gly
NM_001352262.2:c.1213C>G	NP_001339191.1:p.Arg405Gly
NM_025129.5:c.1210C>G MANE Select	NP_079405.2:p.Arg404Gly
NR_033269.2:n.1311C>G