Canonical Allele Identifier: CA1932719239

Gene: SUFU

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504194G= , CM000672.2:g.102504194G=	GRCh38
NC_000010.10:g.104263951G= , CM000672.1:g.104263951G=	GRCh37
NC_000010.9:g.104253941G=	NCBI36
NG_011901.1:g.3562C=
NG_021338.1:g.5233G= , LRG_521:g.5233G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369902.8:c.42G= MANE Select	ENSP00000358918.4:p.Ala14=
ENST00000369899.6:c.42G=	ENSP00000358915.2:p.Ala14=
ENST00000369902.7:c.42G=	ENSP00000358918.3:p.Ala14=
ENST00000423559.2:c.42G=	ENSP00000411597.2:p.Ala14=
NM_001178133.1:c.42G=	NP_001171604.1:p.Ala14=
NM_016169.3:c.42G= , LRG_521t1:c.42G=	NP_057253.2:p.Ala14=
XM_011539858.1:c.42G=	XP_011538160.1:p.Ala14=
XM_011539859.1:c.42G=	XP_011538161.1:p.Ala14=
XM_011539860.1:c.42G=	XP_011538162.1:p.Ala14=
XM_011539861.1:c.42G=	XP_011538163.1:p.Ala14=
XM_011539863.1:c.8+1208G=	XP_011538165.1:n.8+1208G=
XM_011539864.1:c.42G=	XP_011538166.1:p.Ala14=
XM_011539858.3:c.42G=	XP_011538160.1:p.Ala14=
XM_011539860.3:c.42G=	XP_011538162.1:p.Ala14=
XM_011539861.3:c.42G=	XP_011538163.1:p.Ala14=
XM_011539863.3:c.8+1208G=	XP_011538165.1:n.8+1208G=
XM_011539864.3:c.42G=	XP_011538166.1:p.Ala14=
NM_001178133.2:c.42G=	NP_001171604.1:p.Ala14=
NM_016169.4:c.42G= MANE Select	NP_057253.2:p.Ala14=