Canonical Allele Identifier: CA2610694172

Gene: SUFU

Linked Data

• gnomAD v4: 10-102504107-TCGTTTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504109_102504114del , CM000672.2:g.102504109_102504114del	GRCh38
NC_000010.10:g.104263866_104263871del , CM000672.1:g.104263866_104263871del	GRCh37
NC_000010.9:g.104253856_104253861del	NCBI36
NG_011901.1:g.3643_3648del
NG_021338.1:g.5148_5153del , LRG_521:g.5148_5153del

Transcript Alleles

HGVS	Amino-acid change
ENST00000369902.8:c.-44_-39del MANE Select	ENSP00000358918.4:n.-44_-39del
ENST00000369899.6:c.-44_-39del	ENSP00000358915.2:n.-44_-39del
ENST00000369902.7:c.-44_-39del	ENSP00000358918.3:n.-44_-39del
ENST00000423559.2:c.-44_-39del	ENSP00000411597.2:n.-44_-39del
NM_001178133.1:c.-44_-39del	NP_001171604.1:n.-44_-39del
NM_016169.3:c.-44_-39del , LRG_521t1:c.-44_-39del	NP_057253.2:n.-44_-39del
XM_011539858.1:c.-44_-39del	XP_011538160.1:n.-44_-39del
XM_011539859.1:c.-29-15_-29-10del	XP_011538161.1:n.-29-15_-29-10del
XM_011539860.1:c.-44_-39del	XP_011538162.1:n.-44_-39del
XM_011539863.1:c.8+1123_8+1128del	XP_011538165.1:n.8+1123_8+1128del
XM_011539858.3:c.-44_-39del	XP_011538160.1:n.-44_-39del
XM_011539860.3:c.-44_-39del	XP_011538162.1:n.-44_-39del
XM_011539861.3:c.-44_-39del	XP_011538163.1:n.-44_-39del
XM_011539863.3:c.8+1123_8+1128del	XP_011538165.1:n.8+1123_8+1128del
XM_011539864.3:c.-44_-39del	XP_011538166.1:n.-44_-39del
NM_001178133.2:c.-44_-39del	NP_001171604.1:n.-44_-39del
NM_016169.4:c.-44_-39del MANE Select	NP_057253.2:n.-44_-39del