Canonical Allele Identifier: CA2610694140
Gene: SUFU HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102504101_102504102del , CM000672.2:g.102504101_102504102del GRCh38
NC_000010.10:g.104263858_104263859del , CM000672.1:g.104263858_104263859del GRCh37
NC_000010.9:g.104253848_104253849del NCBI36
NG_011901.1:g.3657_3658del
NG_021338.1:g.5140_5141del , LRG_521:g.5140_5141del

Transcript Alleles

HGVS Amino-acid change
ENST00000369902.8:c.-52_-51del MANE Select ENSP00000358918.4:n.-52_-51del
ENST00000369899.6:c.-52_-51del ENSP00000358915.2:n.-52_-51del
ENST00000369902.7:c.-52_-51del ENSP00000358918.3:n.-52_-51del
ENST00000423559.2:c.-52_-51del ENSP00000411597.2:n.-52_-51del
NM_001178133.1:c.-52_-51del NP_001171604.1:n.-52_-51del
NM_016169.3:c.-52_-51del , LRG_521t1:c.-52_-51del NP_057253.2:n.-52_-51del
XM_011539858.1:c.-52_-51del XP_011538160.1:n.-52_-51del
XM_011539859.1:c.-29-23_-29-22del XP_011538161.1:n.-29-23_-29-22del
XM_011539860.1:c.-52_-51del XP_011538162.1:n.-52_-51del
XM_011539863.1:c.8+1115_8+1116del XP_011538165.1:n.8+1115_8+1116del
XM_011539858.3:c.-52_-51del XP_011538160.1:n.-52_-51del
XM_011539860.3:c.-52_-51del XP_011538162.1:n.-52_-51del
XM_011539861.3:c.-52_-51del XP_011538163.1:n.-52_-51del
XM_011539863.3:c.8+1115_8+1116del XP_011538165.1:n.8+1115_8+1116del
XM_011539864.3:c.-52_-51del XP_011538166.1:n.-52_-51del
NM_001178133.2:c.-52_-51del NP_001171604.1:n.-52_-51del
NM_016169.4:c.-52_-51del MANE Select NP_057253.2:n.-52_-51del