Canonical Allele Identifier: CA16612919
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 406387
ClinVar RCV Id: RCV000474581
dbSNP Id: rs1060501108
MyVariant Identifiers: chr10:g.104309750del (hg19) chr10:g.102549993del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102549993del , CM000672.2:g.102549993del GRCh38
NC_000010.10:g.104309750del , CM000672.1:g.104309750del GRCh37
NC_000010.9:g.104299740del NCBI36
NG_021338.1:g.51032del , LRG_521:g.51032del

Transcript Alleles

HGVS Amino-acid change
ENST00000369902.8:c.341del MANE Select ENSP00000358918.4:p.Ser114MetfsTer7
ENST00000369899.6:c.341del ENSP00000358915.2:p.Ser114MetfsTer7
ENST00000369902.7:c.341del ENSP00000358918.3:p.Ser114MetfsTer7
ENST00000423559.2:c.341del ENSP00000411597.2:p.Ser114MetfsTer7
NM_001178133.1:c.341del NP_001171604.1:p.Ser114MetfsTer7
NM_016169.3:c.341del , LRG_521t1:c.341del NP_057253.2:p.Ser114MetfsTer7
XM_011539858.1:c.341del XP_011538160.1:p.Ser114MetfsTer7
XM_011539859.1:c.341del XP_011538161.1:p.Ser114MetfsTer7
XM_011539860.1:c.341del XP_011538162.1:p.Ser114MetfsTer7
XM_011539861.1:c.341del XP_011538163.1:p.Ser114MetfsTer7
XM_011539862.1:c.263del XP_011538164.1:p.Ser88MetfsTer7
XM_011539863.1:c.167del XP_011538165.1:p.Ser56MetfsTer7
XM_011539864.1:c.341del XP_011538166.1:p.Ser114MetfsTer7
XM_011539858.3:c.341del XP_011538160.1:p.Ser114MetfsTer7
XM_011539860.3:c.341del XP_011538162.1:p.Ser114MetfsTer7
XM_011539861.3:c.341del XP_011538163.1:p.Ser114MetfsTer7
XM_011539863.3:c.167del XP_011538165.1:p.Ser56MetfsTer7
XM_011539864.3:c.341del XP_011538166.1:p.Ser114MetfsTer7
XM_017016323.1:c.263del XP_016871812.1:p.Ser88MetfsTer7
NM_001178133.2:c.341del NP_001171604.1:p.Ser114MetfsTer7
NM_016169.4:c.341del MANE Select NP_057253.2:p.Ser114MetfsTer7
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