Canonical Allele Identifier: CA913187385

Gene: SUFU

Linked Data

• ClinVar Variation Id: 1455211
• ClinVar RCV Id: RCV001942253 ; RCV003447612
• dbSNP Id: rs2135597189

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504189_102504205dup , CM000672.2:g.102504189_102504205dup	GRCh38
NC_000010.10:g.104263946_104263962dup , CM000672.1:g.104263946_104263962dup	GRCh37
NC_000010.9:g.104253936_104253952dup	NCBI36
NG_011901.1:g.3565_3581dup
NG_021338.1:g.5228_5244dup , LRG_521:g.5228_5244dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000369902.8:c.37_53dup MANE Select	ENSP00000358918.4:p.Gly19ProfsTer?
ENST00000369899.6:c.37_53dup	ENSP00000358915.2:p.Gly19ProfsTer?
ENST00000369902.7:c.37_53dup	ENSP00000358918.3:p.Gly19ProfsTer?
ENST00000423559.2:c.37_53dup	ENSP00000411597.2:p.Gly19ProfsTer?
NM_001178133.1:c.37_53dup	NP_001171604.1:p.Gly19ProfsTer?
NM_016169.3:c.37_53dup , LRG_521t1:c.37_53dup	NP_057253.2:p.Gly19ProfsTer?
XM_011539858.1:c.37_53dup	XP_011538160.1:p.Gly19ProfsTer?
XM_011539859.1:c.37_53dup	XP_011538161.1:p.Gly19ProfsTer?
XM_011539860.1:c.37_53dup	XP_011538162.1:p.Gly19ProfsTer?
XM_011539861.1:c.37_53dup	XP_011538163.1:p.Gly19ProfsTer?
XM_011539863.1:c.8+1203_8+1219dup	XP_011538165.1:n.8+1203_8+1219dup
XM_011539864.1:c.37_53dup	XP_011538166.1:p.Gly19ProfsTer?
XM_011539858.3:c.37_53dup	XP_011538160.1:p.Gly19ProfsTer?
XM_011539860.3:c.37_53dup	XP_011538162.1:p.Gly19ProfsTer?
XM_011539861.3:c.37_53dup	XP_011538163.1:p.Gly19ProfsTer?
XM_011539863.3:c.8+1203_8+1219dup	XP_011538165.1:n.8+1203_8+1219dup
XM_011539864.3:c.37_53dup	XP_011538166.1:p.Gly19ProfsTer?
NM_001178133.2:c.37_53dup	NP_001171604.1:p.Gly19ProfsTer?
NM_016169.4:c.37_53dup MANE Select	NP_057253.2:p.Gly19ProfsTer?