Canonical Allele Identifier: CA10630822

Gene: SUFU

Linked Data

• ClinVar Variation Id: 298592
• ClinVar RCV Id: RCV000270789
• dbSNP Id: rs117196884
• gnomAD v2: 10-104391584-A-G
• gnomAD v3: 10-102631827-A-G
• gnomAD v4: 10-102631827-A-G
• MyVariant Identifiers: chr10:g.104391584A>G (hg19) ; chr10:g.102631827A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102631827A>G , CM000672.2:g.102631827A>G	GRCh38
NC_000010.10:g.104391584A>G , CM000672.1:g.104391584A>G	GRCh37
NC_000010.9:g.104381574A>G	NCBI36
NG_021338.1:g.132866A>G , LRG_521:g.132866A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369902.8:c.*1672A>G MANE Select	ENSP00000358918.4:n.*1672A>G
ENST00000369902.7:c.*1672A>G	ENSP00000358918.3:n.*1672A>G
NM_016169.3:c.*1672A>G , LRG_521t1:c.*1672A>G	NP_057253.2:n.*1672A>G
XM_011539858.1:c.*1672A>G	XP_011538160.1:n.*1672A>G
XM_011539859.1:c.*1672A>G	XP_011538161.1:n.*1672A>G
XM_011539860.1:c.*1672A>G	XP_011538162.1:n.*1672A>G
XM_011539861.1:c.*1672A>G	XP_011538163.1:n.*1672A>G
XM_011539862.1:c.*1672A>G	XP_011538164.1:n.*1672A>G
XM_011539863.1:c.*1672A>G	XP_011538165.1:n.*1672A>G
XM_011539858.3:c.*1672A>G	XP_011538160.1:n.*1672A>G
XM_011539860.3:c.*1672A>G	XP_011538162.1:n.*1672A>G
XM_011539861.3:c.*1672A>G	XP_011538163.1:n.*1672A>G
XM_011539863.3:c.*1672A>G	XP_011538165.1:n.*1672A>G
XM_017016323.1:c.*1672A>G	XP_016871812.1:n.*1672A>G
NM_016169.4:c.*1672A>G MANE Select	NP_057253.2:n.*1672A>G