Canonical Allele Identifier: CA2002705602
Gene: BUD13 HGNC NCBI

Linked Data

dbSNP Id: rs1940175075

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748301_116748302del , CM000673.2:g.116748301_116748302del GRCh38
NC_000011.9:g.116619017_116619018del , CM000673.1:g.116619017_116619018del GRCh37
NC_000011.8:g.116124227_116124228del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.*180_*181del MANE Select ENSP00000260210.3:n.*180_*181del
ENST00000260210.4:c.*180_*181del ENSP00000260210.3:n.*180_*181del
ENST00000375445.7:c.*180_*181del ENSP00000364594.3:n.*180_*181del
ENST00000419189.1:c.815_816del
NM_001159736.1:c.*180_*181del NP_001153208.1:n.*180_*181del
NM_032725.3:c.*180_*181del NP_116114.1:n.*180_*181del
XM_011543035.1:c.*180_*181del XP_011541337.1:n.*180_*181del
XM_011543035.2:c.*180_*181del XP_011541337.1:n.*180_*181del
NM_032725.4:c.*180_*181del MANE Select NP_116114.1:n.*180_*181del
NM_001159736.2:c.*180_*181del NP_001153208.1:n.*180_*181del