Canonical Allele Identifier: CA2574656408
Gene: SUFU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102504079_102504080del , CM000672.2:g.102504079_102504080del GRCh38
NC_000010.10:g.104263836_104263837del , CM000672.1:g.104263836_104263837del GRCh37
NC_000010.9:g.104253826_104253827del NCBI36
NG_011901.1:g.3677_3678del
NG_021338.1:g.5118_5119del , LRG_521:g.5118_5119del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369902.8:c.-74_-73del MANE Select ENSP00000358918.4:n.-74_-73del
ENST00000369899.6:c.-74_-73del ENSP00000358915.2:n.-74_-73del
ENST00000369902.7:c.-74_-73del ENSP00000358918.3:n.-74_-73del
NM_001178133.1:c.-74_-73del NP_001171604.1:n.-74_-73del
NM_016169.3:c.-74_-73del , LRG_521t1:c.-74_-73del NP_057253.2:n.-74_-73del
XM_011539858.1:c.-74_-73del XP_011538160.1:n.-74_-73del
XM_011539859.1:c.-29-45_-29-44del XP_011538161.1:n.-29-45_-29-44del
XM_011539860.1:c.-74_-73del XP_011538162.1:n.-74_-73del
XM_011539863.1:c.8+1093_8+1094del XP_011538165.1:n.8+1093_8+1094del
XM_011539858.3:c.-74_-73del XP_011538160.1:n.-74_-73del
XM_011539860.3:c.-74_-73del XP_011538162.1:n.-74_-73del
XM_011539861.3:c.-74_-73del XP_011538163.1:n.-74_-73del
XM_011539863.3:c.8+1093_8+1094del XP_011538165.1:n.8+1093_8+1094del
XM_011539864.3:c.-74_-73del XP_011538166.1:n.-74_-73del
NM_001178133.2:c.-74_-73del NP_001171604.1:n.-74_-73del
NM_016169.4:c.-74_-73del MANE Select NP_057253.2:n.-74_-73del