Canonical Allele Identifier: CA659052058

Gene: SUFU

Linked Data

• dbSNP Id: rs1485216756
• gnomAD v3: 10-102504100-C-T
• gnomAD v4: 10-102504100-C-T
• MyVariant Identifiers: chr10:g.104263857C>T (hg19) ; chr10:g.102504100C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504100C>T , CM000672.2:g.102504100C>T	GRCh38
NC_000010.10:g.104263857C>T , CM000672.1:g.104263857C>T	GRCh37
NC_000010.9:g.104253847C>T	NCBI36
NG_011901.1:g.3656G>A
NG_021338.1:g.5139C>T , LRG_521:g.5139C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369902.8:c.-53C>T MANE Select	ENSP00000358918.4:n.-53C>T
ENST00000369899.6:c.-53C>T	ENSP00000358915.2:n.-53C>T
ENST00000369902.7:c.-53C>T	ENSP00000358918.3:n.-53C>T
ENST00000423559.2:c.-53C>T	ENSP00000411597.2:n.-53C>T
NM_001178133.1:c.-53C>T	NP_001171604.1:n.-53C>T
NM_016169.3:c.-53C>T , LRG_521t1:c.-53C>T	NP_057253.2:n.-53C>T
XM_011539858.1:c.-53C>T	XP_011538160.1:n.-53C>T
XM_011539859.1:c.-29-24C>T	XP_011538161.1:n.-29-24C>T
XM_011539860.1:c.-53C>T	XP_011538162.1:n.-53C>T
XM_011539863.1:c.8+1114C>T	XP_011538165.1:n.8+1114C>T
XM_011539858.3:c.-53C>T	XP_011538160.1:n.-53C>T
XM_011539860.3:c.-53C>T	XP_011538162.1:n.-53C>T
XM_011539861.3:c.-53C>T	XP_011538163.1:n.-53C>T
XM_011539863.3:c.8+1114C>T	XP_011538165.1:n.8+1114C>T
XM_011539864.3:c.-53C>T	XP_011538166.1:n.-53C>T
NM_001178133.2:c.-53C>T	NP_001171604.1:n.-53C>T
NM_016169.4:c.-53C>T MANE Select	NP_057253.2:n.-53C>T