Canonical Allele Identifier: CA406900435

Gene: FUZ

Linked Data

• MyVariant Identifiers: chr19:g.50310604T>G (hg19) ; chr19:g.49807347T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49807347T>G , CM000681.2:g.49807347T>G	GRCh38
NC_000019.9:g.50310604T>G , CM000681.1:g.50310604T>G	GRCh37
NC_000019.8:g.55002416T>G	NCBI36
NG_032843.1:g.10964A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313777.9:c.1061A>C MANE Select	ENSP00000313309.4:p.Asp354Ala
ENST00000313777.8:c.1061A>C	ENSP00000313309.4:p.Asp354Ala
ENST00000377092.8:c.*801A>C	ENSP00000366296.5:n.*801A>C
ENST00000525130.5:c.*715A>C	ENSP00000433492.1:n.*715A>C
ENST00000525370.5:c.*718A>C	ENSP00000431420.1:n.*718A>C
ENST00000528094.5:c.953A>C	ENSP00000435177.1:p.Asp318Ala
ENST00000529634.2:c.217A>C
ENST00000533418.5:c.911A>C	ENSP00000431731.1:p.Asp304Ala
NM_001171937.1:c.953A>C	NP_001165408.1:p.Asp318Ala
NM_025129.4:c.1061A>C	NP_079405.2:p.Asp354Ala
NR_033269.1:n.1180A>C
XM_006723399.2:c.*47A>C	XP_006723462.1:n.*47A>C
XM_011527339.1:c.1064A>C	XP_011525641.1:p.Asp355Ala
XM_011527340.1:c.914A>C	XP_011525642.1:p.Asp305Ala
XM_011527341.1:c.914A>C	XP_011525643.1:p.Asp305Ala
XM_011527342.1:c.893A>C	XP_011525644.1:p.Asp298Ala
XM_011527343.1:c.*47A>C	XP_011525645.1:n.*47A>C
XM_011527344.1:c.866A>C	XP_011525646.1:p.Asp289Ala
XM_011527345.1:c.764A>C	XP_011525647.1:p.Asp255Ala
XM_011527346.1:c.764A>C	XP_011525648.1:p.Asp255Ala
XM_011527347.1:c.764A>C	XP_011525649.1:p.Asp255Ala
XR_935862.1:n.1429A>C
NM_001352262.1:c.1064A>C	NP_001339191.1:p.Asp355Ala
NM_001363663.1:c.911A>C	NP_001350592.1:p.Asp304Ala
XM_006723399.3:c.*47A>C	XP_006723462.1:n.*47A>C
XM_011527341.2:c.914A>C	XP_011525643.1:p.Asp305Ala
XM_011527342.2:c.893A>C	XP_011525644.1:p.Asp298Ala
XM_017027321.1:c.761A>C	XP_016882810.1:p.Asp254Ala
XM_017027322.2:c.*47A>C	XP_016882811.1:n.*47A>C
XM_024451729.1:c.893A>C	XP_024307497.1:p.Asp298Ala
XM_024451730.1:c.890A>C	XP_024307498.1:p.Asp297Ala
XR_001753764.1:n.1836A>C
XR_001753765.1:n.1136A>C
XR_002958363.1:n.2087A>C
XR_002958364.1:n.1833A>C
XR_002958365.1:n.1726A>C
NM_001171937.2:c.953A>C	NP_001165408.1:p.Asp318Ala
NM_001352262.2:c.1064A>C	NP_001339191.1:p.Asp355Ala
NM_025129.5:c.1061A>C MANE Select	NP_079405.2:p.Asp354Ala
NR_033269.2:n.1162A>C