Canonical Allele Identifier: CA1932719497
Gene: SUFU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102504262_102504263delinsTC , CM000672.2:g.102504262_102504263delinsTC GRCh38
NC_000010.10:g.104264019_104264020delinsTC , CM000672.1:g.104264019_104264020delinsTC GRCh37
NC_000010.9:g.104254009_104254010delinsTC NCBI36
NG_011901.1:g.3493_3494delinsGA
NG_021338.1:g.5301_5302delinsTC , LRG_521:g.5301_5302delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000369902.8:c.110_111delinsTC MANE Select ENSP00000358918.4:p.Ile37=
ENST00000369899.6:c.110_111delinsTC ENSP00000358915.2:p.Ile37=
ENST00000369902.7:c.110_111delinsTC ENSP00000358918.3:p.Ile37=
ENST00000423559.2:c.110_111delinsTC ENSP00000411597.2:p.Ile37=
NM_001178133.1:c.110_111delinsTC NP_001171604.1:p.Ile37=
NM_016169.3:c.110_111delinsTC , LRG_521t1:c.110_111delinsTC NP_057253.2:p.Ile37=
XM_011539858.1:c.110_111delinsTC XP_011538160.1:p.Ile37=
XM_011539859.1:c.110_111delinsTC XP_011538161.1:p.Ile37=
XM_011539860.1:c.110_111delinsTC XP_011538162.1:p.Ile37=
XM_011539861.1:c.110_111delinsTC XP_011538163.1:p.Ile37=
XM_011539862.1:c.-106_-105delinsTC XP_011538164.1:n.-106_-105delinsTC
XM_011539863.1:c.8+1276_8+1277delinsTC XP_011538165.1:n.8+1276_8+1277delinsTC
XM_011539864.1:c.110_111delinsTC XP_011538166.1:p.Ile37=
XM_011539858.3:c.110_111delinsTC XP_011538160.1:p.Ile37=
XM_011539860.3:c.110_111delinsTC XP_011538162.1:p.Ile37=
XM_011539861.3:c.110_111delinsTC XP_011538163.1:p.Ile37=
XM_011539863.3:c.8+1276_8+1277delinsTC XP_011538165.1:n.8+1276_8+1277delinsTC
XM_011539864.3:c.110_111delinsTC XP_011538166.1:p.Ile37=
NM_001178133.2:c.110_111delinsTC NP_001171604.1:p.Ile37=
NM_016169.4:c.110_111delinsTC MANE Select NP_057253.2:p.Ile37=