Canonical Allele Identifier: CA16612722

Gene: SUFU

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102630129G>A , CM000672.2:g.102630129G>A	GRCh38
NC_000010.10:g.104389886G>A , CM000672.1:g.104389886G>A	GRCh37
NC_000010.9:g.104379876G>A	NCBI36
NG_021338.1:g.131168G>A , LRG_521:g.131168G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_016169.4:c.1429G>A MANE Select	NP_057253.2:p.Val477Met
ENST00000369902.8:c.1429G>A MANE Select	ENSP00000358918.4:p.Val477Met
NM_016169.3:c.1429G>A , LRG_521t1:c.1429G>A	NP_057253.2:p.Val477Met
ENST00000369902.7:c.1429G>A	ENSP00000358918.3:p.Val477Met
XM_011539858.1:c.1558G>A	XP_011538160.1:p.Val520Met
XM_011539858.3:c.1558G>A	XP_011538160.1:p.Val520Met
XM_011539859.1:c.1558G>A	XP_011538161.1:p.Val520Met
XM_011539860.1:c.1555G>A	XP_011538162.1:p.Val519Met
XM_011539860.3:c.1555G>A	XP_011538162.1:p.Val519Met
XM_011539861.1:c.1432G>A	XP_011538163.1:p.Val478Met
XM_011539861.3:c.1432G>A	XP_011538163.1:p.Val478Met
XM_011539862.1:c.1480G>A	XP_011538164.1:p.Val494Met
XM_011539863.1:c.1384G>A	XP_011538165.1:p.Val462Met
XM_011539863.3:c.1384G>A	XP_011538165.1:p.Val462Met
XM_017016323.1:c.1480G>A	XP_016871812.1:p.Val494Met