Canonical Allele Identifier: CA5667912

Gene: SUFU

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102617405G>A , CM000672.2:g.102617405G>A	GRCh38
NC_000010.10:g.104377162G>A , CM000672.1:g.104377162G>A	GRCh37
NC_000010.9:g.104367152G>A	NCBI36
NG_021338.1:g.118444G>A , LRG_521:g.118444G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_016169.4:c.1273G>A MANE Select	NP_057253.2:p.Ala425Thr
ENST00000369902.8:c.1273G>A MANE Select	ENSP00000358918.4:p.Ala425Thr
NM_001178133.1:c.1273G>A	NP_001171604.1:p.Ala425Thr
NM_001178133.2:c.1273G>A	NP_001171604.1:p.Ala425Thr
NM_016169.3:c.1273G>A , LRG_521t1:c.1273G>A	NP_057253.2:p.Ala425Thr
ENST00000369899.6:c.1273G>A	ENSP00000358915.2:p.Ala425Thr
ENST00000369902.7:c.1273G>A	ENSP00000358918.3:p.Ala425Thr
ENST00000423559.2:c.1273G>A	ENSP00000411597.2:p.Ala425Thr
XM_011539858.1:c.1276G>A	XP_011538160.1:p.Ala426Thr
XM_011539858.3:c.1276G>A	XP_011538160.1:p.Ala426Thr
XM_011539859.1:c.1276G>A	XP_011538161.1:p.Ala426Thr
XM_011539860.1:c.1273G>A	XP_011538162.1:p.Ala425Thr
XM_011539860.3:c.1273G>A	XP_011538162.1:p.Ala425Thr
XM_011539861.1:c.1276G>A	XP_011538163.1:p.Ala426Thr
XM_011539861.3:c.1276G>A	XP_011538163.1:p.Ala426Thr
XM_011539862.1:c.1198G>A	XP_011538164.1:p.Ala400Thr
XM_011539863.1:c.1102G>A	XP_011538165.1:p.Ala368Thr
XM_011539863.3:c.1102G>A	XP_011538165.1:p.Ala368Thr
XM_011539864.1:c.1276G>A	XP_011538166.1:p.Ala426Thr
XM_011539864.3:c.1276G>A	XP_011538166.1:p.Ala426Thr
XM_017016323.1:c.1198G>A	XP_016871812.1:p.Ala400Thr