Canonical Allele Identifier: CA659052198

Gene: SUFU

Linked Data

• ClinVar Variation Id: 835932
• ClinVar RCV Id: RCV001036934
• dbSNP Id: rs1426839991
• gnomAD v3: 10-102504194-GCCCCCGGCCCCTGGCCCGACTGCC-G
• gnomAD v4: 10-102504194-GCCCCCGGCCCCTGGCCCGACTGCC-G
• MyVariant Identifiers: chr10:g.104263952_104263975del (hg19) ; chr10:g.102504195_102504218del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504204_102504227del , CM000672.2:g.102504204_102504227del	GRCh38
NC_000010.10:g.104263961_104263984del , CM000672.1:g.104263961_104263984del	GRCh37
NC_000010.9:g.104253951_104253974del	NCBI36
NG_011901.1:g.3538_3561del
NG_021338.1:g.5243_5266del , LRG_521:g.5243_5266del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369902.8:c.52_75del MANE Select	ENSP00000358918.4:p.Pro18_Ala25del
ENST00000369899.6:c.52_75del	ENSP00000358915.2:p.Pro18_Ala25del
ENST00000369902.7:c.52_75del	ENSP00000358918.3:p.Pro18_Ala25del
ENST00000423559.2:c.52_75del	ENSP00000411597.2:p.Pro18_Ala25del
NM_001178133.1:c.52_75del	NP_001171604.1:p.Pro18_Ala25del
NM_016169.3:c.52_75del , LRG_521t1:c.52_75del	NP_057253.2:p.Pro18_Ala25del
XM_011539858.1:c.52_75del	XP_011538160.1:p.Pro18_Ala25del
XM_011539859.1:c.52_75del	XP_011538161.1:p.Pro18_Ala25del
XM_011539860.1:c.52_75del	XP_011538162.1:p.Pro18_Ala25del
XM_011539861.1:c.52_75del	XP_011538163.1:p.Pro18_Ala25del
XM_011539863.1:c.8+1218_8+1241del	XP_011538165.1:n.8+1218_8+1241del
XM_011539864.1:c.52_75del	XP_011538166.1:p.Pro18_Ala25del
XM_011539858.3:c.52_75del	XP_011538160.1:p.Pro18_Ala25del
XM_011539860.3:c.52_75del	XP_011538162.1:p.Pro18_Ala25del
XM_011539861.3:c.52_75del	XP_011538163.1:p.Pro18_Ala25del
XM_011539863.3:c.8+1218_8+1241del	XP_011538165.1:n.8+1218_8+1241del
XM_011539864.3:c.52_75del	XP_011538166.1:p.Pro18_Ala25del
NM_001178133.2:c.52_75del	NP_001171604.1:p.Pro18_Ala25del
NM_016169.4:c.52_75del MANE Select	NP_057253.2:p.Pro18_Ala25del