Canonical Allele Identifier: CA2722590721
Gene: SUFU HGNC NCBI

Linked Data

dbSNP Id: rs2135596640

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102504096T>G , CM000672.2:g.102504096T>G GRCh38
NC_000010.10:g.104263853T>G , CM000672.1:g.104263853T>G GRCh37
NC_000010.9:g.104253843T>G NCBI36
NG_011901.1:g.3660A>C
NG_021338.1:g.5135T>G , LRG_521:g.5135T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369902.8:c.-57T>G MANE Select ENSP00000358918.4:n.-57T>G
ENST00000369899.6:c.-57T>G ENSP00000358915.2:n.-57T>G
ENST00000369902.7:c.-57T>G ENSP00000358918.3:n.-57T>G
ENST00000423559.2:c.-57T>G ENSP00000411597.2:n.-57T>G
NM_001178133.1:c.-57T>G NP_001171604.1:n.-57T>G
NM_016169.3:c.-57T>G , LRG_521t1:c.-57T>G NP_057253.2:n.-57T>G
XM_011539858.1:c.-57T>G XP_011538160.1:n.-57T>G
XM_011539859.1:c.-29-28T>G XP_011538161.1:n.-29-28T>G
XM_011539860.1:c.-57T>G XP_011538162.1:n.-57T>G
XM_011539863.1:c.8+1110T>G XP_011538165.1:n.8+1110T>G
XM_011539858.3:c.-57T>G XP_011538160.1:n.-57T>G
XM_011539860.3:c.-57T>G XP_011538162.1:n.-57T>G
XM_011539861.3:c.-57T>G XP_011538163.1:n.-57T>G
XM_011539863.3:c.8+1110T>G XP_011538165.1:n.8+1110T>G
XM_011539864.3:c.-57T>G XP_011538166.1:n.-57T>G
NM_001178133.2:c.-57T>G NP_001171604.1:n.-57T>G
NM_016169.4:c.-57T>G MANE Select NP_057253.2:n.-57T>G