Canonical Allele Identifier: CA1932718845

Gene: SUFU

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504003_102504014delinsAGTGCGCCGTGC , CM000672.2:g.102504003_102504014delinsAGTGCGCCGTGC	GRCh38
NC_000010.10:g.104263760_104263771delinsAGTGCGCCGTGC , CM000672.1:g.104263760_104263771delinsAGTGCGCCGTGC	GRCh37
NC_000010.9:g.104253750_104253761delinsAGTGCGCCGTGC	NCBI36
NG_011901.1:g.3742_3753delinsGCACGGCGCACT
NG_021338.1:g.5042_5053delinsAGTGCGCCGTGC , LRG_521:g.5042_5053delinsAGTGCGCCGTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369902.8:c.-150_-139delinsAGTGCGCCGTGC MANE Select	ENSP00000358918.4:n.-150_-139delinsAGTGCGCCGTGC
ENST00000369902.7:c.-150_-139delinsAGTGCGCCGTGC	ENSP00000358918.3:n.-150_-139delinsAGTGCGCCGTGC
NM_001178133.1:c.-150_-139delinsAGTGCGCCGTGC	NP_001171604.1:n.-150_-139delinsAGTGCGCCGTGC
NM_016169.3:c.-150_-139delinsAGTGCGCCGTGC , LRG_521t1:c.-150_-139delinsAGTGCGCCGTGC	NP_057253.2:n.-150_-139delinsAGTGCGCCGTGC
XM_011539858.1:c.-150_-139delinsAGTGCGCCGTGC	XP_011538160.1:n.-150_-139delinsAGTGCGCCGTGC
XM_011539859.1:c.-29-121_-29-110delinsAGTGCGCCGTGC	XP_011538161.1:n.-29-121_-29-110delinsAGTGCGCCGTGC
XM_011539860.1:c.-150_-139delinsAGTGCGCCGTGC	XP_011538162.1:n.-150_-139delinsAGTGCGCCGTGC
XM_011539863.1:c.8+1017_8+1028delinsAGTGCGCCGTGC	XP_011538165.1:n.8+1017_8+1028delinsAGTGCGCCGTGC
XM_011539858.3:c.-150_-139delinsAGTGCGCCGTGC	XP_011538160.1:n.-150_-139delinsAGTGCGCCGTGC
XM_011539860.3:c.-150_-139delinsAGTGCGCCGTGC	XP_011538162.1:n.-150_-139delinsAGTGCGCCGTGC
XM_011539861.3:c.-150_-139delinsAGTGCGCCGTGC	XP_011538163.1:n.-150_-139delinsAGTGCGCCGTGC
XM_011539863.3:c.8+1017_8+1028delinsAGTGCGCCGTGC	XP_011538165.1:n.8+1017_8+1028delinsAGTGCGCCGTGC
XM_011539864.3:c.-150_-139delinsAGTGCGCCGTGC	XP_011538166.1:n.-150_-139delinsAGTGCGCCGTGC
NM_001178133.2:c.-150_-139delinsAGTGCGCCGTGC	NP_001171604.1:n.-150_-139delinsAGTGCGCCGTGC
NM_016169.4:c.-150_-139delinsAGTGCGCCGTGC MANE Select	NP_057253.2:n.-150_-139delinsAGTGCGCCGTGC