Canonical Allele Identifier: CA1932722398

Gene: SUFU

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102549993G= , CM000672.2:g.102549993G=	GRCh38
NC_000010.10:g.104309750G= , CM000672.1:g.104309750G=	GRCh37
NC_000010.9:g.104299740G=	NCBI36
NG_021338.1:g.51032G= , LRG_521:g.51032G=

Transcript Alleles

HGVS	Amino-acid Change
NM_016169.4:c.341G= MANE Select	NP_057253.2:p.Ser114=
ENST00000369902.8:c.341G= MANE Select	ENSP00000358918.4:p.Ser114=
NM_001178133.1:c.341G=	NP_001171604.1:p.Ser114=
NM_001178133.2:c.341G=	NP_001171604.1:p.Ser114=
NM_016169.3:c.341G= , LRG_521t1:c.341G=	NP_057253.2:p.Ser114=
ENST00000369899.6:c.341G=	ENSP00000358915.2:p.Ser114=
ENST00000369902.7:c.341G=	ENSP00000358918.3:p.Ser114=
ENST00000423559.2:c.341G=	ENSP00000411597.2:p.Ser114=
XM_011539858.1:c.341G=	XP_011538160.1:p.Ser114=
XM_011539858.3:c.341G=	XP_011538160.1:p.Ser114=
XM_011539859.1:c.341G=	XP_011538161.1:p.Ser114=
XM_011539860.1:c.341G=	XP_011538162.1:p.Ser114=
XM_011539860.3:c.341G=	XP_011538162.1:p.Ser114=
XM_011539861.1:c.341G=	XP_011538163.1:p.Ser114=
XM_011539861.3:c.341G=	XP_011538163.1:p.Ser114=
XM_011539862.1:c.263G=	XP_011538164.1:p.Ser88=
XM_011539863.1:c.167G=	XP_011538165.1:p.Ser56=
XM_011539863.3:c.167G=	XP_011538165.1:p.Ser56=
XM_011539864.1:c.341G=	XP_011538166.1:p.Ser114=
XM_011539864.3:c.341G=	XP_011538166.1:p.Ser114=
XM_017016323.1:c.263G=	XP_016871812.1:p.Ser88=