Canonical Allele Identifier: CA2722358714
Gene: SUFU HGNC NCBI

Linked Data

dbSNP Id: rs1332258864

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102504181_102504182dup , CM000672.2:g.102504181_102504182dup GRCh38
NC_000010.10:g.104263938_104263939dup , CM000672.1:g.104263938_104263939dup GRCh37
NC_000010.9:g.104253928_104253929dup NCBI36
NG_011901.1:g.3577_3578dup
NG_021338.1:g.5220_5221dup , LRG_521:g.5220_5221dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369902.8:c.29_30dup MANE Select ENSP00000358918.4:p.Gly11ProfsTer?
ENST00000369899.6:c.29_30dup ENSP00000358915.2:p.Gly11ProfsTer?
ENST00000369902.7:c.29_30dup ENSP00000358918.3:p.Gly11ProfsTer?
ENST00000423559.2:c.29_30dup ENSP00000411597.2:p.Gly11ProfsTer?
NM_001178133.1:c.29_30dup NP_001171604.1:p.Gly11ProfsTer?
NM_016169.3:c.29_30dup , LRG_521t1:c.29_30dup NP_057253.2:p.Gly11ProfsTer?
XM_011539858.1:c.29_30dup XP_011538160.1:p.Gly11ProfsTer?
XM_011539859.1:c.29_30dup XP_011538161.1:p.Gly11ProfsTer?
XM_011539860.1:c.29_30dup XP_011538162.1:p.Gly11ProfsTer?
XM_011539861.1:c.29_30dup XP_011538163.1:p.Gly11ProfsTer?
XM_011539863.1:c.8+1195_8+1196dup XP_011538165.1:n.8+1195_8+1196dup
XM_011539864.1:c.29_30dup XP_011538166.1:p.Gly11ProfsTer?
XM_011539858.3:c.29_30dup XP_011538160.1:p.Gly11ProfsTer?
XM_011539860.3:c.29_30dup XP_011538162.1:p.Gly11ProfsTer?
XM_011539861.3:c.29_30dup XP_011538163.1:p.Gly11ProfsTer?
XM_011539863.3:c.8+1195_8+1196dup XP_011538165.1:n.8+1195_8+1196dup
XM_011539864.3:c.29_30dup XP_011538166.1:p.Gly11ProfsTer?
NM_001178133.2:c.29_30dup NP_001171604.1:p.Gly11ProfsTer?
NM_016169.4:c.29_30dup MANE Select NP_057253.2:p.Gly11ProfsTer?