Canonical Allele Identifier: CA377920366

Gene: SUFU

Linked Data

• ClinVar Variation Id: 1343419
• ClinVar RCV Id: RCV001844437
• dbSNP Id: rs2135959354
• COSMIC: COSM4011297
• MyVariant Identifiers: chr10:g.104389822G>A (hg19) ; chr10:g.102630065G>A (hg38)
• MutSpliceDB: CA377920366

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102630065G>A , CM000672.2:g.102630065G>A	GRCh38
NC_000010.10:g.104389822G>A , CM000672.1:g.104389822G>A	GRCh37
NC_000010.9:g.104379812G>A	NCBI36
NG_021338.1:g.131104G>A , LRG_521:g.131104G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369902.8:c.1366-1G>A MANE Select	ENSP00000358918.4:n.1366-1G>A
ENST00000369902.7:c.1366-1G>A	ENSP00000358918.3:n.1366-1G>A
NM_016169.3:c.1366-1G>A , LRG_521t1:c.1366-1G>A	NP_057253.2:n.1366-1G>A
XM_011539858.1:c.1495-1G>A	XP_011538160.1:n.1495-1G>A
XM_011539859.1:c.1495-1G>A	XP_011538161.1:n.1495-1G>A
XM_011539860.1:c.1492-1G>A	XP_011538162.1:n.1492-1G>A
XM_011539861.1:c.1369-1G>A	XP_011538163.1:n.1369-1G>A
XM_011539862.1:c.1417-1G>A	XP_011538164.1:n.1417-1G>A
XM_011539863.1:c.1321-1G>A	XP_011538165.1:n.1321-1G>A
XM_011539858.3:c.1495-1G>A	XP_011538160.1:n.1495-1G>A
XM_011539860.3:c.1492-1G>A	XP_011538162.1:n.1492-1G>A
XM_011539861.3:c.1369-1G>A	XP_011538163.1:n.1369-1G>A
XM_011539863.3:c.1321-1G>A	XP_011538165.1:n.1321-1G>A
XM_017016323.1:c.1417-1G>A	XP_016871812.1:n.1417-1G>A
NM_016169.4:c.1366-1G>A MANE Select	NP_057253.2:n.1366-1G>A