Canonical Allele Identifier: CA2610694088
Gene: SUFU HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102504081_102504082dup , CM000672.2:g.102504081_102504082dup GRCh38
NC_000010.10:g.104263838_104263839dup , CM000672.1:g.104263838_104263839dup GRCh37
NC_000010.9:g.104253828_104253829dup NCBI36
NG_011901.1:g.3675_3676dup
NG_021338.1:g.5120_5121dup , LRG_521:g.5120_5121dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369902.8:c.-72_-71dup MANE Select ENSP00000358918.4:n.-72_-71dup
ENST00000369899.6:c.-72_-71dup ENSP00000358915.2:n.-72_-71dup
ENST00000369902.7:c.-72_-71dup ENSP00000358918.3:n.-72_-71dup
ENST00000423559.2:c.-72_-71dup ENSP00000411597.2:n.-72_-71dup
NM_001178133.1:c.-72_-71dup NP_001171604.1:n.-72_-71dup
NM_016169.3:c.-72_-71dup , LRG_521t1:c.-72_-71dup NP_057253.2:n.-72_-71dup
XM_011539858.1:c.-72_-71dup XP_011538160.1:n.-72_-71dup
XM_011539859.1:c.-29-43_-29-42dup XP_011538161.1:n.-29-43_-29-42dup
XM_011539860.1:c.-72_-71dup XP_011538162.1:n.-72_-71dup
XM_011539863.1:c.8+1095_8+1096dup XP_011538165.1:n.8+1095_8+1096dup
XM_011539858.3:c.-72_-71dup XP_011538160.1:n.-72_-71dup
XM_011539860.3:c.-72_-71dup XP_011538162.1:n.-72_-71dup
XM_011539861.3:c.-72_-71dup XP_011538163.1:n.-72_-71dup
XM_011539863.3:c.8+1095_8+1096dup XP_011538165.1:n.8+1095_8+1096dup
XM_011539864.3:c.-72_-71dup XP_011538166.1:n.-72_-71dup
NM_001178133.2:c.-72_-71dup NP_001171604.1:n.-72_-71dup
NM_016169.4:c.-72_-71dup MANE Select NP_057253.2:n.-72_-71dup