Canonical Allele Identifier: CA2002705859
Gene: BUD13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748461_116748462delinsAC , CM000673.2:g.116748461_116748462delinsAC GRCh38
NC_000011.9:g.116619177_116619178delinsAC , CM000673.1:g.116619177_116619178delinsAC GRCh37
NC_000011.8:g.116124387_116124388delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.*20_*21delinsGT MANE Select ENSP00000260210.3:n.*20_*21delinsGT
ENST00000260210.4:c.*20_*21delinsGT ENSP00000260210.3:n.*20_*21delinsGT
ENST00000375445.7:c.*20_*21delinsGT ENSP00000364594.3:n.*20_*21delinsGT
ENST00000419189.1:c.655_656delinsGT
NM_001159736.1:c.*20_*21delinsGT NP_001153208.1:n.*20_*21delinsGT
NM_032725.3:c.*20_*21delinsGT NP_116114.1:n.*20_*21delinsGT
XM_011543035.1:c.*20_*21delinsGT XP_011541337.1:n.*20_*21delinsGT
XM_011543035.2:c.*20_*21delinsGT XP_011541337.1:n.*20_*21delinsGT
NM_032725.4:c.*20_*21delinsGT MANE Select NP_116114.1:n.*20_*21delinsGT
NM_001159736.2:c.*20_*21delinsGT NP_001153208.1:n.*20_*21delinsGT