Canonical Allele Identifier: CA1932718860

Gene: SUFU

Linked Data

• dbSNP Id: rs2062285031
• gnomAD v4: 10-102504007-CGCCGTGCGCAGGCGCGGAGCTAGACCTCGCTGCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504011_102504044del , CM000672.2:g.102504011_102504044del	GRCh38
NC_000010.10:g.104263768_104263801del , CM000672.1:g.104263768_104263801del	GRCh37
NC_000010.9:g.104253758_104253791del	NCBI36
NG_011901.1:g.3715_3748del
NG_021338.1:g.5050_5083del , LRG_521:g.5050_5083del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369902.8:c.-142_-109del MANE Select	ENSP00000358918.4:n.-142_-109del
ENST00000369899.6:c.-142_-109del	ENSP00000358915.2:n.-142_-109del
ENST00000369902.7:c.-142_-109del	ENSP00000358918.3:n.-142_-109del
NM_001178133.1:c.-142_-109del	NP_001171604.1:n.-142_-109del
NM_016169.3:c.-142_-109del , LRG_521t1:c.-142_-109del	NP_057253.2:n.-142_-109del
XM_011539858.1:c.-142_-109del	XP_011538160.1:n.-142_-109del
XM_011539859.1:c.-29-113_-29-80del	XP_011538161.1:n.-29-113_-29-80del
XM_011539860.1:c.-142_-109del	XP_011538162.1:n.-142_-109del
XM_011539863.1:c.8+1025_8+1058del	XP_011538165.1:n.8+1025_8+1058del
XM_011539858.3:c.-142_-109del	XP_011538160.1:n.-142_-109del
XM_011539860.3:c.-142_-109del	XP_011538162.1:n.-142_-109del
XM_011539861.3:c.-142_-109del	XP_011538163.1:n.-142_-109del
XM_011539863.3:c.8+1025_8+1058del	XP_011538165.1:n.8+1025_8+1058del
XM_011539864.3:c.-142_-109del	XP_011538166.1:n.-142_-109del
NM_001178133.2:c.-142_-109del	NP_001171604.1:n.-142_-109del
NM_016169.4:c.-142_-109del MANE Select	NP_057253.2:n.-142_-109del