Canonical Allele Identifier: CA1932719330
Gene: SUFU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102504210C= , CM000672.2:g.102504210C= GRCh38
NC_000010.10:g.104263967C= , CM000672.1:g.104263967C= GRCh37
NC_000010.9:g.104253957C= NCBI36
NG_011901.1:g.3546G=
NG_021338.1:g.5249C= , LRG_521:g.5249C=

Transcript Alleles

HGVS Amino-acid change
ENST00000369902.8:c.58C= MANE Select ENSP00000358918.4:p.Pro20=
ENST00000369899.6:c.58C= ENSP00000358915.2:p.Pro20=
ENST00000369902.7:c.58C= ENSP00000358918.3:p.Pro20=
ENST00000423559.2:c.58C= ENSP00000411597.2:p.Pro20=
NM_001178133.1:c.58C= NP_001171604.1:p.Pro20=
NM_016169.3:c.58C= , LRG_521t1:c.58C= NP_057253.2:p.Pro20=
XM_011539858.1:c.58C= XP_011538160.1:p.Pro20=
XM_011539859.1:c.58C= XP_011538161.1:p.Pro20=
XM_011539860.1:c.58C= XP_011538162.1:p.Pro20=
XM_011539861.1:c.58C= XP_011538163.1:p.Pro20=
XM_011539863.1:c.8+1224C= XP_011538165.1:n.8+1224C=
XM_011539864.1:c.58C= XP_011538166.1:p.Pro20=
XM_011539858.3:c.58C= XP_011538160.1:p.Pro20=
XM_011539860.3:c.58C= XP_011538162.1:p.Pro20=
XM_011539861.3:c.58C= XP_011538163.1:p.Pro20=
XM_011539863.3:c.8+1224C= XP_011538165.1:n.8+1224C=
XM_011539864.3:c.58C= XP_011538166.1:p.Pro20=
NM_001178133.2:c.58C= NP_001171604.1:p.Pro20=
NM_016169.4:c.58C= MANE Select NP_057253.2:p.Pro20=