Canonical Allele Identifier: CA2610694191

Gene: SUFU

Linked Data

• gnomAD v4: 10-102504113-GCCCTCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504116_102504121del , CM000672.2:g.102504116_102504121del	GRCh38
NC_000010.10:g.104263873_104263878del , CM000672.1:g.104263873_104263878del	GRCh37
NC_000010.9:g.104253863_104253868del	NCBI36
NG_011901.1:g.3637_3642del
NG_021338.1:g.5155_5160del , LRG_521:g.5155_5160del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369902.8:c.-37_-32del MANE Select	ENSP00000358918.4:n.-37_-32del
ENST00000369899.6:c.-37_-32del	ENSP00000358915.2:n.-37_-32del
ENST00000369902.7:c.-37_-32del	ENSP00000358918.3:n.-37_-32del
ENST00000423559.2:c.-37_-32del	ENSP00000411597.2:n.-37_-32del
NM_001178133.1:c.-37_-32del	NP_001171604.1:n.-37_-32del
NM_016169.3:c.-37_-32del , LRG_521t1:c.-37_-32del	NP_057253.2:n.-37_-32del
XM_011539858.1:c.-37_-32del	XP_011538160.1:n.-37_-32del
XM_011539859.1:c.-29-8_-29-3del	XP_011538161.1:n.-29-8_-29-3del
XM_011539860.1:c.-37_-32del	XP_011538162.1:n.-37_-32del
XM_011539863.1:c.8+1130_8+1135del	XP_011538165.1:n.8+1130_8+1135del
XM_011539858.3:c.-37_-32del	XP_011538160.1:n.-37_-32del
XM_011539860.3:c.-37_-32del	XP_011538162.1:n.-37_-32del
XM_011539861.3:c.-37_-32del	XP_011538163.1:n.-37_-32del
XM_011539863.3:c.8+1130_8+1135del	XP_011538165.1:n.8+1130_8+1135del
XM_011539864.3:c.-37_-32del	XP_011538166.1:n.-37_-32del
NM_001178133.2:c.-37_-32del	NP_001171604.1:n.-37_-32del
NM_016169.4:c.-37_-32del MANE Select	NP_057253.2:n.-37_-32del