Canonical Allele Identifier: CA2002715087
Gene: BUD13 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116755450T= , CM000673.2:g.116755450T= GRCh38
NC_000011.9:g.116626166T= , CM000673.1:g.116626166T= GRCh37
NC_000011.8:g.116131376T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260210.5:c.1766+1696A= MANE Select ENSP00000260210.3:n.1766+1696A=
ENST00000260210.4:c.1766+1696A= ENSP00000260210.3:n.1766+1696A=
ENST00000375445.7:c.1364+1696A= ENSP00000364594.3:n.1364+1696A=
ENST00000419189.1:c.541+1696A=
NM_001159736.1:c.1364+1696A= NP_001153208.1:n.1364+1696A=
NM_032725.3:c.1766+1696A= NP_116114.1:n.1766+1696A=
XM_011543035.1:c.1667+1696A= XP_011541337.1:n.1667+1696A=
XM_011543035.2:c.1667+1696A= XP_011541337.1:n.1667+1696A=
NM_032725.4:c.1766+1696A= MANE Select NP_116114.1:n.1766+1696A=
NM_001159736.2:c.1364+1696A= NP_001153208.1:n.1364+1696A=
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