Canonical Allele Identifier: CA595210468

Gene: SUFU

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102630058C>T , CM000672.2:g.102630058C>T	GRCh38
NC_000010.10:g.104389815C>T , CM000672.1:g.104389815C>T	GRCh37
NC_000010.9:g.104379805C>T	NCBI36
NG_021338.1:g.131097C>T , LRG_521:g.131097C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_016169.4:c.1366-8C>T MANE Select	NP_057253.2:n.1366-8C>T
ENST00000369902.8:c.1366-8C>T MANE Select	ENSP00000358918.4:n.1366-8C>T
NM_016169.3:c.1366-8C>T , LRG_521t1:c.1366-8C>T	NP_057253.2:n.1366-8C>T
ENST00000369902.7:c.1366-8C>T	ENSP00000358918.3:n.1366-8C>T
XM_011539858.1:c.1495-8C>T	XP_011538160.1:n.1495-8C>T
XM_011539858.3:c.1495-8C>T	XP_011538160.1:n.1495-8C>T
XM_011539859.1:c.1495-8C>T	XP_011538161.1:n.1495-8C>T
XM_011539860.1:c.1492-8C>T	XP_011538162.1:n.1492-8C>T
XM_011539860.3:c.1492-8C>T	XP_011538162.1:n.1492-8C>T
XM_011539861.1:c.1369-8C>T	XP_011538163.1:n.1369-8C>T
XM_011539861.3:c.1369-8C>T	XP_011538163.1:n.1369-8C>T
XM_011539862.1:c.1417-8C>T	XP_011538164.1:n.1417-8C>T
XM_011539863.1:c.1321-8C>T	XP_011538165.1:n.1321-8C>T
XM_011539863.3:c.1321-8C>T	XP_011538165.1:n.1321-8C>T
XM_017016323.1:c.1417-8C>T	XP_016871812.1:n.1417-8C>T