Canonical Allele Identifier: CA1932772796

Gene: SUFU

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102599545G= , CM000672.2:g.102599545G=	GRCh38
NC_000010.10:g.104359302G= , CM000672.1:g.104359302G=	GRCh37
NC_000010.9:g.104349292G=	NCBI36
NG_021338.1:g.100584G= , LRG_521:g.100584G=

Transcript Alleles

HGVS	Amino-acid Change
NM_016169.4:c.1022+1G= MANE Select	NP_057253.2:n.1022+1G=
ENST00000369902.8:c.1022+1G= MANE Select	ENSP00000358918.4:n.1022+1G=
NM_001178133.1:c.1022+1G=	NP_001171604.1:n.1022+1G=
NM_001178133.2:c.1022+1G=	NP_001171604.1:n.1022+1G=
NM_016169.3:c.1022+1G= , LRG_521t1:c.1022+1G=	NP_057253.2:n.1022+1G=
ENST00000369899.6:c.1022+1G=	ENSP00000358915.2:n.1022+1G=
ENST00000369902.7:c.1022+1G=	ENSP00000358918.3:n.1022+1G=
ENST00000423559.2:c.1022+1G=	ENSP00000411597.2:n.1022+1G=
XM_011539858.1:c.1025+1G=	XP_011538160.1:n.1025+1G=
XM_011539858.3:c.1025+1G=	XP_011538160.1:n.1025+1G=
XM_011539859.1:c.1025+1G=	XP_011538161.1:n.1025+1G=
XM_011539860.1:c.1022+1G=	XP_011538162.1:n.1022+1G=
XM_011539860.3:c.1022+1G=	XP_011538162.1:n.1022+1G=
XM_011539861.1:c.1025+1G=	XP_011538163.1:n.1025+1G=
XM_011539861.3:c.1025+1G=	XP_011538163.1:n.1025+1G=
XM_011539862.1:c.947+1G=	XP_011538164.1:n.947+1G=
XM_011539863.1:c.851+1G=	XP_011538165.1:n.851+1G=
XM_011539863.3:c.851+1G=	XP_011538165.1:n.851+1G=
XM_011539864.1:c.1025+1G=	XP_011538166.1:n.1025+1G=
XM_011539864.3:c.1025+1G=	XP_011538166.1:n.1025+1G=
XM_017016323.1:c.947+1G=	XP_016871812.1:n.947+1G=