Canonical Allele Identifier: CA595216477

Gene: SUFU

Linked Data

• dbSNP Id: rs1332258864
• gnomAD v2: 10-104263934-G-GC
• gnomAD v4: 10-102504177-G-GC
• MyVariant Identifiers: chr10:g.104263934_104263935insC (hg19) ; chr10:g.102504177_102504178insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504182dup , CM000672.2:g.102504182dup	GRCh38
NC_000010.10:g.104263939dup , CM000672.1:g.104263939dup	GRCh37
NC_000010.9:g.104253929dup	NCBI36
NG_011901.1:g.3578dup
NG_021338.1:g.5221dup , LRG_521:g.5221dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369902.8:c.30dup MANE Select	ENSP00000358918.4:p.Gly11ArgfsTer?
ENST00000369899.6:c.30dup	ENSP00000358915.2:p.Gly11ArgfsTer?
ENST00000369902.7:c.30dup	ENSP00000358918.3:p.Gly11ArgfsTer?
ENST00000423559.2:c.30dup	ENSP00000411597.2:p.Gly11ArgfsTer?
NM_001178133.1:c.30dup	NP_001171604.1:p.Gly11ArgfsTer?
NM_016169.3:c.30dup , LRG_521t1:c.30dup	NP_057253.2:p.Gly11ArgfsTer?
XM_011539858.1:c.30dup	XP_011538160.1:p.Gly11ArgfsTer?
XM_011539859.1:c.30dup	XP_011538161.1:p.Gly11ArgfsTer?
XM_011539860.1:c.30dup	XP_011538162.1:p.Gly11ArgfsTer?
XM_011539861.1:c.30dup	XP_011538163.1:p.Gly11ArgfsTer?
XM_011539863.1:c.8+1196dup	XP_011538165.1:n.8+1196dup
XM_011539864.1:c.30dup	XP_011538166.1:p.Gly11ArgfsTer?
XM_011539858.3:c.30dup	XP_011538160.1:p.Gly11ArgfsTer?
XM_011539860.3:c.30dup	XP_011538162.1:p.Gly11ArgfsTer?
XM_011539861.3:c.30dup	XP_011538163.1:p.Gly11ArgfsTer?
XM_011539863.3:c.8+1196dup	XP_011538165.1:n.8+1196dup
XM_011539864.3:c.30dup	XP_011538166.1:p.Gly11ArgfsTer?
NM_001178133.2:c.30dup	NP_001171604.1:p.Gly11ArgfsTer?
NM_016169.4:c.30dup MANE Select	NP_057253.2:p.Gly11ArgfsTer?