Canonical Allele Identifier: CA2002705599
Gene: BUD13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748300_116748302delinsGAA , CM000673.2:g.116748300_116748302delinsGAA GRCh38
NC_000011.9:g.116619016_116619018delinsGAA , CM000673.1:g.116619016_116619018delinsGAA GRCh37
NC_000011.8:g.116124226_116124228delinsGAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.*180_*182delinsTTC MANE Select ENSP00000260210.3:n.*180_*182delinsTTC
ENST00000260210.4:c.*180_*182delinsTTC ENSP00000260210.3:n.*180_*182delinsTTC
ENST00000375445.7:c.*180_*182delinsTTC ENSP00000364594.3:n.*180_*182delinsTTC
ENST00000419189.1:c.815_817delinsTTC
NM_001159736.1:c.*180_*182delinsTTC NP_001153208.1:n.*180_*182delinsTTC
NM_032725.3:c.*180_*182delinsTTC NP_116114.1:n.*180_*182delinsTTC
XM_011543035.1:c.*180_*182delinsTTC XP_011541337.1:n.*180_*182delinsTTC
XM_011543035.2:c.*180_*182delinsTTC XP_011541337.1:n.*180_*182delinsTTC
NM_032725.4:c.*180_*182delinsTTC MANE Select NP_116114.1:n.*180_*182delinsTTC
NM_001159736.2:c.*180_*182delinsTTC NP_001153208.1:n.*180_*182delinsTTC