Canonical Allele Identifier: CA377918805

Gene: SUFU

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102627213G>T , CM000672.2:g.102627213G>T	GRCh38
NC_000010.10:g.104386970G>T , CM000672.1:g.104386970G>T	GRCh37
NC_000010.9:g.104376960G>T	NCBI36
NG_021338.1:g.128252G>T , LRG_521:g.128252G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_016169.4:c.1335G>T MANE Select	NP_057253.2:p.Glu445Asp
ENST00000369902.8:c.1335G>T MANE Select	ENSP00000358918.4:p.Glu445Asp
NM_016169.3:c.1335G>T , LRG_521t1:c.1335G>T	NP_057253.2:p.Glu445Asp
ENST00000369902.7:c.1335G>T	ENSP00000358918.3:p.Glu445Asp
XM_011539858.1:c.1464G>T	XP_011538160.1:p.Glu488Asp
XM_011539858.3:c.1464G>T	XP_011538160.1:p.Glu488Asp
XM_011539859.1:c.1464G>T	XP_011538161.1:p.Glu488Asp
XM_011539860.1:c.1461G>T	XP_011538162.1:p.Glu487Asp
XM_011539860.3:c.1461G>T	XP_011538162.1:p.Glu487Asp
XM_011539861.1:c.1338G>T	XP_011538163.1:p.Glu446Asp
XM_011539861.3:c.1338G>T	XP_011538163.1:p.Glu446Asp
XM_011539862.1:c.1386G>T	XP_011538164.1:p.Glu462Asp
XM_011539863.1:c.1290G>T	XP_011538165.1:p.Glu430Asp
XM_011539863.3:c.1290G>T	XP_011538165.1:p.Glu430Asp
XM_017016323.1:c.1386G>T	XP_016871812.1:p.Glu462Asp