Canonical Allele Identifier: CA5667799

Gene: SUFU

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102597277G>T , CM000672.2:g.102597277G>T	GRCh38
NC_000010.10:g.104357034G>T , CM000672.1:g.104357034G>T	GRCh37
NC_000010.9:g.104347024G>T	NCBI36
NG_021338.1:g.98316G>T , LRG_521:g.98316G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_016169.4:c.894G>T MANE Select	NP_057253.2:p.Arg298=
ENST00000369902.8:c.894G>T MANE Select	ENSP00000358918.4:p.Arg298=
NM_001178133.1:c.894G>T	NP_001171604.1:p.Arg298=
NM_001178133.2:c.894G>T	NP_001171604.1:p.Arg298=
NM_016169.3:c.894G>T , LRG_521t1:c.894G>T	NP_057253.2:p.Arg298=
ENST00000369899.6:c.894G>T	ENSP00000358915.2:p.Arg298=
ENST00000369902.7:c.894G>T	ENSP00000358918.3:p.Arg298=
ENST00000423559.2:c.894G>T	ENSP00000411597.2:p.Arg298=
ENST00000471000.1:n.676G>T
XM_011539858.1:c.897G>T	XP_011538160.1:p.Arg299=
XM_011539858.3:c.897G>T	XP_011538160.1:p.Arg299=
XM_011539859.1:c.897G>T	XP_011538161.1:p.Arg299=
XM_011539860.1:c.894G>T	XP_011538162.1:p.Arg298=
XM_011539860.3:c.894G>T	XP_011538162.1:p.Arg298=
XM_011539861.1:c.897G>T	XP_011538163.1:p.Arg299=
XM_011539861.3:c.897G>T	XP_011538163.1:p.Arg299=
XM_011539862.1:c.819G>T	XP_011538164.1:p.Arg273=
XM_011539863.1:c.723G>T	XP_011538165.1:p.Arg241=
XM_011539863.3:c.723G>T	XP_011538165.1:p.Arg241=
XM_011539864.1:c.897G>T	XP_011538166.1:p.Arg299=
XM_011539864.3:c.897G>T	XP_011538166.1:p.Arg299=
XM_017016323.1:c.819G>T	XP_016871812.1:p.Arg273=