Canonical Allele Identifier: CA2610694436
Gene: SUFU HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102504280_102504282del , CM000672.2:g.102504280_102504282del GRCh38
NC_000010.10:g.104264037_104264039del , CM000672.1:g.104264037_104264039del GRCh37
NC_000010.9:g.104254027_104254029del NCBI36
NG_011901.1:g.3480_3482del
NG_021338.1:g.5319_5321del , LRG_521:g.5319_5321del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369902.8:c.128_130del MANE Select ENSP00000358918.4:p.Arg43del
ENST00000369899.6:c.128_130del ENSP00000358915.2:p.Arg43del
ENST00000369902.7:c.128_130del ENSP00000358918.3:p.Arg43del
ENST00000423559.2:c.128_130del ENSP00000411597.2:p.Arg43del
NM_001178133.1:c.128_130del NP_001171604.1:p.Arg43del
NM_016169.3:c.128_130del , LRG_521t1:c.128_130del NP_057253.2:p.Arg43del
XM_011539858.1:c.128_130del XP_011538160.1:p.Arg43del
XM_011539859.1:c.128_130del XP_011538161.1:p.Arg43del
XM_011539860.1:c.128_130del XP_011538162.1:p.Arg43del
XM_011539861.1:c.128_130del XP_011538163.1:p.Arg43del
XM_011539862.1:c.-88_-86del XP_011538164.1:n.-88_-86del
XM_011539863.1:c.8+1294_8+1296del XP_011538165.1:n.8+1294_8+1296del
XM_011539864.1:c.128_130del XP_011538166.1:p.Arg43del
XM_011539858.3:c.128_130del XP_011538160.1:p.Arg43del
XM_011539860.3:c.128_130del XP_011538162.1:p.Arg43del
XM_011539861.3:c.128_130del XP_011538163.1:p.Arg43del
XM_011539863.3:c.8+1294_8+1296del XP_011538165.1:n.8+1294_8+1296del
XM_011539864.3:c.128_130del XP_011538166.1:p.Arg43del
NM_001178133.2:c.128_130del NP_001171604.1:p.Arg43del
NM_016169.4:c.128_130del MANE Select NP_057253.2:p.Arg43del