Canonical Allele Identifier: CA2610694419
Gene: SUFU HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102504188_102504189insCCCCCCCC , CM000672.2:g.102504188_102504189insCCCCCCCC GRCh38
NC_000010.10:g.104263945_104263946insCCCCCCCC , CM000672.1:g.104263945_104263946insCCCCCCCC GRCh37
NC_000010.9:g.104253935_104253936insCCCCCCCC NCBI36
NG_011901.1:g.3571_3572insGGGGGGGG
NG_021338.1:g.5227_5228insCCCCCCCC , LRG_521:g.5227_5228insCCCCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000369902.8:c.36_37insCCCCCCCC MANE Select ENSP00000358918.4:p.Thr13ProfsTer?
ENST00000369899.6:c.36_37insCCCCCCCC ENSP00000358915.2:p.Thr13ProfsTer?
ENST00000369902.7:c.36_37insCCCCCCCC ENSP00000358918.3:p.Thr13ProfsTer?
ENST00000423559.2:c.36_37insCCCCCCCC ENSP00000411597.2:p.Thr13ProfsTer?
NM_001178133.1:c.36_37insCCCCCCCC NP_001171604.1:p.Thr13ProfsTer?
NM_016169.3:c.36_37insCCCCCCCC , LRG_521t1:c.36_37insCCCCCCCC NP_057253.2:p.Thr13ProfsTer?
XM_011539858.1:c.36_37insCCCCCCCC XP_011538160.1:p.Thr13ProfsTer?
XM_011539859.1:c.36_37insCCCCCCCC XP_011538161.1:p.Thr13ProfsTer?
XM_011539860.1:c.36_37insCCCCCCCC XP_011538162.1:p.Thr13ProfsTer?
XM_011539861.1:c.36_37insCCCCCCCC XP_011538163.1:p.Thr13ProfsTer?
XM_011539863.1:c.8+1202_8+1203insCCCCCCCC XP_011538165.1:n.8+1202_8+1203insCCCCCCCC
XM_011539864.1:c.36_37insCCCCCCCC XP_011538166.1:p.Thr13ProfsTer?
XM_011539858.3:c.36_37insCCCCCCCC XP_011538160.1:p.Thr13ProfsTer?
XM_011539860.3:c.36_37insCCCCCCCC XP_011538162.1:p.Thr13ProfsTer?
XM_011539861.3:c.36_37insCCCCCCCC XP_011538163.1:p.Thr13ProfsTer?
XM_011539863.3:c.8+1202_8+1203insCCCCCCCC XP_011538165.1:n.8+1202_8+1203insCCCCCCCC
XM_011539864.3:c.36_37insCCCCCCCC XP_011538166.1:p.Thr13ProfsTer?
NM_001178133.2:c.36_37insCCCCCCCC NP_001171604.1:p.Thr13ProfsTer?
NM_016169.4:c.36_37insCCCCCCCC MANE Select NP_057253.2:p.Thr13ProfsTer?