Canonical Allele Identifier: CA2825001676

Gene: SUFU

Linked Data

• ClinVar Variation Id: 3226875
• ClinVar RCV Id: RCV004522041

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504174_102504190del , CM000672.2:g.102504174_102504190del	GRCh38
NC_000010.10:g.104263931_104263947del , CM000672.1:g.104263931_104263947del	GRCh37
NC_000010.9:g.104253921_104253937del	NCBI36
NG_011901.1:g.3567_3583del
NG_021338.1:g.5213_5229del , LRG_521:g.5213_5229del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369902.8:c.22_38del MANE Select	ENSP00000358918.4:p.Gly8ArgfsTer?
ENST00000369899.6:c.22_38del	ENSP00000358915.2:p.Gly8ArgfsTer?
ENST00000369902.7:c.22_38del	ENSP00000358918.3:p.Gly8ArgfsTer?
ENST00000423559.2:c.22_38del	ENSP00000411597.2:p.Gly8ArgfsTer?
NM_001178133.1:c.22_38del	NP_001171604.1:p.Gly8ArgfsTer?
NM_016169.3:c.22_38del , LRG_521t1:c.22_38del	NP_057253.2:p.Gly8ArgfsTer?
XM_011539858.1:c.22_38del	XP_011538160.1:p.Gly8ArgfsTer?
XM_011539859.1:c.22_38del	XP_011538161.1:p.Gly8ArgfsTer?
XM_011539860.1:c.22_38del	XP_011538162.1:p.Gly8ArgfsTer?
XM_011539861.1:c.22_38del	XP_011538163.1:p.Gly8ArgfsTer?
XM_011539863.1:c.8+1188_8+1204del	XP_011538165.1:n.8+1188_8+1204del
XM_011539864.1:c.22_38del	XP_011538166.1:p.Gly8ArgfsTer?
XM_011539858.3:c.22_38del	XP_011538160.1:p.Gly8ArgfsTer?
XM_011539860.3:c.22_38del	XP_011538162.1:p.Gly8ArgfsTer?
XM_011539861.3:c.22_38del	XP_011538163.1:p.Gly8ArgfsTer?
XM_011539863.3:c.8+1188_8+1204del	XP_011538165.1:n.8+1188_8+1204del
XM_011539864.3:c.22_38del	XP_011538166.1:p.Gly8ArgfsTer?
NM_001178133.2:c.22_38del	NP_001171604.1:p.Gly8ArgfsTer?
NM_016169.4:c.22_38del MANE Select	NP_057253.2:p.Gly8ArgfsTer?