Canonical Allele Identifier: CA2002705677
Gene: BUD13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748347G= , CM000673.2:g.116748347G= GRCh38
NC_000011.9:g.116619063G= , CM000673.1:g.116619063G= GRCh37
NC_000011.8:g.116124273G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260210.5:c.*135C= MANE Select ENSP00000260210.3:n.*135C=
ENST00000260210.4:c.*135C= ENSP00000260210.3:n.*135C=
ENST00000375445.7:c.*135C= ENSP00000364594.3:n.*135C=
ENST00000419189.1:c.770C=
NM_001159736.1:c.*135C= NP_001153208.1:n.*135C=
NM_032725.3:c.*135C= NP_116114.1:n.*135C=
XM_011543035.1:c.*135C= XP_011541337.1:n.*135C=
XM_011543035.2:c.*135C= XP_011541337.1:n.*135C=
NM_032725.4:c.*135C= MANE Select NP_116114.1:n.*135C=
NM_001159736.2:c.*135C= NP_001153208.1:n.*135C=