Canonical Allele Identifier: CA931939943
Gene: SUFU HGNC NCBI

Linked Data

dbSNP Id: rs2062286055

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102504059G>A , CM000672.2:g.102504059G>A GRCh38
NC_000010.10:g.104263816G>A , CM000672.1:g.104263816G>A GRCh37
NC_000010.9:g.104253806G>A NCBI36
NG_011901.1:g.3697C>T
NG_021338.1:g.5098G>A , LRG_521:g.5098G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369902.8:c.-94G>A MANE Select ENSP00000358918.4:n.-94G>A
ENST00000369899.6:c.-94G>A ENSP00000358915.2:n.-94G>A
ENST00000369902.7:c.-94G>A ENSP00000358918.3:n.-94G>A
NM_001178133.1:c.-94G>A NP_001171604.1:n.-94G>A
NM_016169.3:c.-94G>A , LRG_521t1:c.-94G>A NP_057253.2:n.-94G>A
XM_011539858.1:c.-94G>A XP_011538160.1:n.-94G>A
XM_011539859.1:c.-29-65G>A XP_011538161.1:n.-29-65G>A
XM_011539860.1:c.-94G>A XP_011538162.1:n.-94G>A
XM_011539863.1:c.8+1073G>A XP_011538165.1:n.8+1073G>A
XM_011539858.3:c.-94G>A XP_011538160.1:n.-94G>A
XM_011539860.3:c.-94G>A XP_011538162.1:n.-94G>A
XM_011539861.3:c.-94G>A XP_011538163.1:n.-94G>A
XM_011539863.3:c.8+1073G>A XP_011538165.1:n.8+1073G>A
XM_011539864.3:c.-94G>A XP_011538166.1:n.-94G>A
NM_001178133.2:c.-94G>A NP_001171604.1:n.-94G>A
NM_016169.4:c.-94G>A MANE Select NP_057253.2:n.-94G>A