Canonical Allele Identifier: CA659052061

Gene: SUFU

Linked Data

• dbSNP Id: rs1262881383
• gnomAD v3: 10-102504101-T-A
• gnomAD v4: 10-102504101-T-A
• MyVariant Identifiers: chr10:g.104263858T>A (hg19) ; chr10:g.102504101T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504101T>A , CM000672.2:g.102504101T>A	GRCh38
NC_000010.10:g.104263858T>A , CM000672.1:g.104263858T>A	GRCh37
NC_000010.9:g.104253848T>A	NCBI36
NG_011901.1:g.3655A>T
NG_021338.1:g.5140T>A , LRG_521:g.5140T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000369902.8:c.-52T>A MANE Select	ENSP00000358918.4:n.-52T>A
ENST00000369899.6:c.-52T>A	ENSP00000358915.2:n.-52T>A
ENST00000369902.7:c.-52T>A	ENSP00000358918.3:n.-52T>A
ENST00000423559.2:c.-52T>A	ENSP00000411597.2:n.-52T>A
NM_001178133.1:c.-52T>A	NP_001171604.1:n.-52T>A
NM_016169.3:c.-52T>A , LRG_521t1:c.-52T>A	NP_057253.2:n.-52T>A
XM_011539858.1:c.-52T>A	XP_011538160.1:n.-52T>A
XM_011539859.1:c.-29-23T>A	XP_011538161.1:n.-29-23T>A
XM_011539860.1:c.-52T>A	XP_011538162.1:n.-52T>A
XM_011539863.1:c.8+1115T>A	XP_011538165.1:n.8+1115T>A
XM_011539858.3:c.-52T>A	XP_011538160.1:n.-52T>A
XM_011539860.3:c.-52T>A	XP_011538162.1:n.-52T>A
XM_011539861.3:c.-52T>A	XP_011538163.1:n.-52T>A
XM_011539863.3:c.8+1115T>A	XP_011538165.1:n.8+1115T>A
XM_011539864.3:c.-52T>A	XP_011538166.1:n.-52T>A
NM_001178133.2:c.-52T>A	NP_001171604.1:n.-52T>A
NM_016169.4:c.-52T>A MANE Select	NP_057253.2:n.-52T>A