Canonical Allele Identifier: CA16612826

Gene: SUFU

Linked Data

• ClinVar Variation Id: 406381
• ClinVar RCV Id: RCV000472343 ; RCV003448312
• dbSNP Id: rs1060501105
• MyVariant Identifiers: chr10:g.104375023A>T (hg19) ; chr10:g.102615266A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102615266A>T , CM000672.2:g.102615266A>T	GRCh38
NC_000010.10:g.104375023A>T , CM000672.1:g.104375023A>T	GRCh37
NC_000010.9:g.104365013A>T	NCBI36
NG_021338.1:g.116305A>T , LRG_521:g.116305A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369902.8:c.1023-2A>T MANE Select	ENSP00000358918.4:n.1023-2A>T
ENST00000369899.6:c.1023-2A>T	ENSP00000358915.2:n.1023-2A>T
ENST00000369902.7:c.1023-2A>T	ENSP00000358918.3:n.1023-2A>T
ENST00000423559.2:c.1023-2A>T	ENSP00000411597.2:n.1023-2A>T
NM_001178133.1:c.1023-2A>T	NP_001171604.1:n.1023-2A>T
NM_016169.3:c.1023-2A>T , LRG_521t1:c.1023-2A>T	NP_057253.2:n.1023-2A>T
XM_011539858.1:c.1026-2A>T	XP_011538160.1:n.1026-2A>T
XM_011539859.1:c.1026-2A>T	XP_011538161.1:n.1026-2A>T
XM_011539860.1:c.1023-2A>T	XP_011538162.1:n.1023-2A>T
XM_011539861.1:c.1026-2A>T	XP_011538163.1:n.1026-2A>T
XM_011539862.1:c.948-2A>T	XP_011538164.1:n.948-2A>T
XM_011539863.1:c.852-2A>T	XP_011538165.1:n.852-2A>T
XM_011539864.1:c.1026-2A>T	XP_011538166.1:n.1026-2A>T
XM_011539858.3:c.1026-2A>T	XP_011538160.1:n.1026-2A>T
XM_011539860.3:c.1023-2A>T	XP_011538162.1:n.1023-2A>T
XM_011539861.3:c.1026-2A>T	XP_011538163.1:n.1026-2A>T
XM_011539863.3:c.852-2A>T	XP_011538165.1:n.852-2A>T
XM_011539864.3:c.1026-2A>T	XP_011538166.1:n.1026-2A>T
XM_017016323.1:c.948-2A>T	XP_016871812.1:n.948-2A>T
NM_001178133.2:c.1023-2A>T	NP_001171604.1:n.1023-2A>T
NM_016169.4:c.1023-2A>T MANE Select	NP_057253.2:n.1023-2A>T