Canonical Allele Identifier: CA377886474

Gene: SUFU

Linked Data

• ClinVar Variation Id: 1773688
• ClinVar RCV Id: RCV003095227 ; RCV003313277 ; RCV002389605 ; RCV003464518
• dbSNP Id: rs2135598180
• gnomAD v4: 10-102504255-C-T
• MyVariant Identifiers: chr10:g.104264012C>T (hg19) ; chr10:g.102504255C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504255C>T , CM000672.2:g.102504255C>T	GRCh38
NC_000010.10:g.104264012C>T , CM000672.1:g.104264012C>T	GRCh37
NC_000010.9:g.104254002C>T	NCBI36
NG_011901.1:g.3501G>A
NG_021338.1:g.5294C>T , LRG_521:g.5294C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369902.8:c.103C>T MANE Select	ENSP00000358918.4:p.His35Tyr
ENST00000369899.6:c.103C>T	ENSP00000358915.2:p.His35Tyr
ENST00000369902.7:c.103C>T	ENSP00000358918.3:p.His35Tyr
ENST00000423559.2:c.103C>T	ENSP00000411597.2:p.His35Tyr
NM_001178133.1:c.103C>T	NP_001171604.1:p.His35Tyr
NM_016169.3:c.103C>T , LRG_521t1:c.103C>T	NP_057253.2:p.His35Tyr
XM_011539858.1:c.103C>T	XP_011538160.1:p.His35Tyr
XM_011539859.1:c.103C>T	XP_011538161.1:p.His35Tyr
XM_011539860.1:c.103C>T	XP_011538162.1:p.His35Tyr
XM_011539861.1:c.103C>T	XP_011538163.1:p.His35Tyr
XM_011539862.1:c.-113C>T	XP_011538164.1:n.-113C>T
XM_011539863.1:c.8+1269C>T	XP_011538165.1:n.8+1269C>T
XM_011539864.1:c.103C>T	XP_011538166.1:p.His35Tyr
XM_011539858.3:c.103C>T	XP_011538160.1:p.His35Tyr
XM_011539860.3:c.103C>T	XP_011538162.1:p.His35Tyr
XM_011539861.3:c.103C>T	XP_011538163.1:p.His35Tyr
XM_011539863.3:c.8+1269C>T	XP_011538165.1:n.8+1269C>T
XM_011539864.3:c.103C>T	XP_011538166.1:p.His35Tyr
NM_001178133.2:c.103C>T	NP_001171604.1:p.His35Tyr
NM_016169.4:c.103C>T MANE Select	NP_057253.2:p.His35Tyr