Canonical Allele Identifier: CA942596661
Gene: BUD13 HGNC NCBI

Linked Data

dbSNP Id: rs1940306234

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116755472del , CM000673.2:g.116755472del GRCh38
NC_000011.9:g.116626188del , CM000673.1:g.116626188del GRCh37
NC_000011.8:g.116131398del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1766+1674del MANE Select ENSP00000260210.3:n.1766+1674del
ENST00000260210.4:c.1766+1674del ENSP00000260210.3:n.1766+1674del
ENST00000375445.7:c.1364+1674del ENSP00000364594.3:n.1364+1674del
ENST00000419189.1:c.541+1674del
NM_001159736.1:c.1364+1674del NP_001153208.1:n.1364+1674del
NM_032725.3:c.1766+1674del NP_116114.1:n.1766+1674del
XM_011543035.1:c.1667+1674del XP_011541337.1:n.1667+1674del
XM_011543035.2:c.1667+1674del XP_011541337.1:n.1667+1674del
NM_032725.4:c.1766+1674del MANE Select NP_116114.1:n.1766+1674del
NM_001159736.2:c.1364+1674del NP_001153208.1:n.1364+1674del