Canonical Allele Identifier: CA931939909

Gene: SUFU

Linked Data

• dbSNP Id: rs2062284843
• gnomAD v3: 10-102504003-AGTGCGCCGTGC-A
• gnomAD v4: 10-102504003-AGTGCGCCGTGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504005_102504015del , CM000672.2:g.102504005_102504015del	GRCh38
NC_000010.10:g.104263762_104263772del , CM000672.1:g.104263762_104263772del	GRCh37
NC_000010.9:g.104253752_104253762del	NCBI36
NG_011901.1:g.3742_3752del
NG_021338.1:g.5044_5054del , LRG_521:g.5044_5054del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369902.8:c.-148_-138del MANE Select	ENSP00000358918.4:n.-148_-138del
ENST00000369902.7:c.-148_-138del	ENSP00000358918.3:n.-148_-138del
NM_001178133.1:c.-148_-138del	NP_001171604.1:n.-148_-138del
NM_016169.3:c.-148_-138del , LRG_521t1:c.-148_-138del	NP_057253.2:n.-148_-138del
XM_011539858.1:c.-148_-138del	XP_011538160.1:n.-148_-138del
XM_011539859.1:c.-29-119_-29-109del	XP_011538161.1:n.-29-119_-29-109del
XM_011539860.1:c.-148_-138del	XP_011538162.1:n.-148_-138del
XM_011539863.1:c.8+1019_8+1029del	XP_011538165.1:n.8+1019_8+1029del
XM_011539858.3:c.-148_-138del	XP_011538160.1:n.-148_-138del
XM_011539860.3:c.-148_-138del	XP_011538162.1:n.-148_-138del
XM_011539861.3:c.-148_-138del	XP_011538163.1:n.-148_-138del
XM_011539863.3:c.8+1019_8+1029del	XP_011538165.1:n.8+1019_8+1029del
XM_011539864.3:c.-148_-138del	XP_011538166.1:n.-148_-138del
NM_001178133.2:c.-148_-138del	NP_001171604.1:n.-148_-138del
NM_016169.4:c.-148_-138del MANE Select	NP_057253.2:n.-148_-138del