Canonical Allele Identifier: CA377918835

Gene: SUFU

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102627225T>G , CM000672.2:g.102627225T>G	GRCh38
NC_000010.10:g.104386982T>G , CM000672.1:g.104386982T>G	GRCh37
NC_000010.9:g.104376972T>G	NCBI36
NG_021338.1:g.128264T>G , LRG_521:g.128264T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_016169.4:c.1347T>G MANE Select	NP_057253.2:p.Asp449Glu
ENST00000369902.8:c.1347T>G MANE Select	ENSP00000358918.4:p.Asp449Glu
NM_016169.3:c.1347T>G , LRG_521t1:c.1347T>G	NP_057253.2:p.Asp449Glu
ENST00000369902.7:c.1347T>G	ENSP00000358918.3:p.Asp449Glu
XM_011539858.1:c.1476T>G	XP_011538160.1:p.Asp492Glu
XM_011539858.3:c.1476T>G	XP_011538160.1:p.Asp492Glu
XM_011539859.1:c.1476T>G	XP_011538161.1:p.Asp492Glu
XM_011539860.1:c.1473T>G	XP_011538162.1:p.Asp491Glu
XM_011539860.3:c.1473T>G	XP_011538162.1:p.Asp491Glu
XM_011539861.1:c.1350T>G	XP_011538163.1:p.Asp450Glu
XM_011539861.3:c.1350T>G	XP_011538163.1:p.Asp450Glu
XM_011539862.1:c.1398T>G	XP_011538164.1:p.Asp466Glu
XM_011539863.1:c.1302T>G	XP_011538165.1:p.Asp434Glu
XM_011539863.3:c.1302T>G	XP_011538165.1:p.Asp434Glu
XM_017016323.1:c.1398T>G	XP_016871812.1:p.Asp466Glu