Canonical Allele Identifier: CA377886340
Gene: SUFU HGNC NCBI

Linked Data

ClinVar Variation Id: 2930271
ClinVar RCV Id: RCV003787629
dbSNP Id: rs1219870817

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102504222C>A , CM000672.2:g.102504222C>A GRCh38
NC_000010.10:g.104263979C>A , CM000672.1:g.104263979C>A GRCh37
NC_000010.9:g.104253969C>A NCBI36
NG_011901.1:g.3534G>T
NG_021338.1:g.5261C>A , LRG_521:g.5261C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369902.8:c.70C>A MANE Select ENSP00000358918.4:p.Pro24Thr
ENST00000369899.6:c.70C>A ENSP00000358915.2:p.Pro24Thr
ENST00000369902.7:c.70C>A ENSP00000358918.3:p.Pro24Thr
ENST00000423559.2:c.70C>A ENSP00000411597.2:p.Pro24Thr
NM_001178133.1:c.70C>A NP_001171604.1:p.Pro24Thr
NM_016169.3:c.70C>A , LRG_521t1:c.70C>A NP_057253.2:p.Pro24Thr
XM_011539858.1:c.70C>A XP_011538160.1:p.Pro24Thr
XM_011539859.1:c.70C>A XP_011538161.1:p.Pro24Thr
XM_011539860.1:c.70C>A XP_011538162.1:p.Pro24Thr
XM_011539861.1:c.70C>A XP_011538163.1:p.Pro24Thr
XM_011539863.1:c.8+1236C>A XP_011538165.1:n.8+1236C>A
XM_011539864.1:c.70C>A XP_011538166.1:p.Pro24Thr
XM_011539858.3:c.70C>A XP_011538160.1:p.Pro24Thr
XM_011539860.3:c.70C>A XP_011538162.1:p.Pro24Thr
XM_011539861.3:c.70C>A XP_011538163.1:p.Pro24Thr
XM_011539863.3:c.8+1236C>A XP_011538165.1:n.8+1236C>A
XM_011539864.3:c.70C>A XP_011538166.1:p.Pro24Thr
NM_001178133.2:c.70C>A NP_001171604.1:p.Pro24Thr
NM_016169.4:c.70C>A MANE Select NP_057253.2:p.Pro24Thr