Canonical Allele Identifier: CA377909686

Gene: SUFU

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102593991A>G , CM000672.2:g.102593991A>G	GRCh38
NC_000010.10:g.104353748A>G , CM000672.1:g.104353748A>G	GRCh37
NC_000010.9:g.104343738A>G	NCBI36
NG_021338.1:g.95030A>G , LRG_521:g.95030A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_016169.4:c.684-2A>G MANE Select	NP_057253.2:n.684-2A>G
ENST00000369902.8:c.684-2A>G MANE Select	ENSP00000358918.4:n.684-2A>G
NM_001178133.1:c.684-2A>G	NP_001171604.1:n.684-2A>G
NM_001178133.2:c.684-2A>G	NP_001171604.1:n.684-2A>G
NM_016169.3:c.684-2A>G , LRG_521t1:c.684-2A>G	NP_057253.2:n.684-2A>G
ENST00000369899.6:c.684-2A>G	ENSP00000358915.2:n.684-2A>G
ENST00000369902.7:c.684-2A>G	ENSP00000358918.3:n.684-2A>G
ENST00000423559.2:c.684-2A>G	ENSP00000411597.2:n.684-2A>G
ENST00000471000.1:n.466-2A>G
XM_011539858.1:c.684-2A>G	XP_011538160.1:n.684-2A>G
XM_011539858.3:c.684-2A>G	XP_011538160.1:n.684-2A>G
XM_011539859.1:c.684-2A>G	XP_011538161.1:n.684-2A>G
XM_011539860.1:c.684-2A>G	XP_011538162.1:n.684-2A>G
XM_011539860.3:c.684-2A>G	XP_011538162.1:n.684-2A>G
XM_011539861.1:c.684-2A>G	XP_011538163.1:n.684-2A>G
XM_011539861.3:c.684-2A>G	XP_011538163.1:n.684-2A>G
XM_011539862.1:c.606-2A>G	XP_011538164.1:n.606-2A>G
XM_011539863.1:c.510-2A>G	XP_011538165.1:n.510-2A>G
XM_011539863.3:c.510-2A>G	XP_011538165.1:n.510-2A>G
XM_011539864.1:c.684-2A>G	XP_011538166.1:n.684-2A>G
XM_011539864.3:c.684-2A>G	XP_011538166.1:n.684-2A>G
XM_017016323.1:c.606-2A>G	XP_016871812.1:n.606-2A>G