Canonical Allele Identifier: CA377918877

Gene: SUFU

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102627244G>A , CM000672.2:g.102627244G>A	GRCh38
NC_000010.10:g.104387001G>A , CM000672.1:g.104387001G>A	GRCh37
NC_000010.9:g.104376991G>A	NCBI36
NG_021338.1:g.128283G>A , LRG_521:g.128283G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_016169.4:c.1365+1G>A MANE Select	NP_057253.2:n.1365+1G>A
ENST00000369902.8:c.1365+1G>A MANE Select	ENSP00000358918.4:n.1365+1G>A
NM_016169.3:c.1365+1G>A , LRG_521t1:c.1365+1G>A	NP_057253.2:n.1365+1G>A
ENST00000369902.7:c.1365+1G>A	ENSP00000358918.3:n.1365+1G>A
XM_011539858.1:c.1494+1G>A	XP_011538160.1:n.1494+1G>A
XM_011539858.3:c.1494+1G>A	XP_011538160.1:n.1494+1G>A
XM_011539859.1:c.1494+1G>A	XP_011538161.1:n.1494+1G>A
XM_011539860.1:c.1491+1G>A	XP_011538162.1:n.1491+1G>A
XM_011539860.3:c.1491+1G>A	XP_011538162.1:n.1491+1G>A
XM_011539861.1:c.1368+1G>A	XP_011538163.1:n.1368+1G>A
XM_011539861.3:c.1368+1G>A	XP_011538163.1:n.1368+1G>A
XM_011539862.1:c.1416+1G>A	XP_011538164.1:n.1416+1G>A
XM_011539863.1:c.1320+1G>A	XP_011538165.1:n.1320+1G>A
XM_011539863.3:c.1320+1G>A	XP_011538165.1:n.1320+1G>A
XM_017016323.1:c.1416+1G>A	XP_016871812.1:n.1416+1G>A