Canonical Allele Identifier: CA2002706270
Gene: BUD13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748686T= , CM000673.2:g.116748686T= GRCh38
NC_000011.9:g.116619402T= , CM000673.1:g.116619402T= GRCh37
NC_000011.8:g.116124612T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1767-111A= MANE Select ENSP00000260210.3:n.1767-111A=
ENST00000260210.4:c.1767-111A= ENSP00000260210.3:n.1767-111A=
ENST00000375445.7:c.1365-111A= ENSP00000364594.3:n.1365-111A=
ENST00000419189.1:c.542-111A=
NM_001159736.1:c.1365-111A= NP_001153208.1:n.1365-111A=
NM_032725.3:c.1767-111A= NP_116114.1:n.1767-111A=
XM_011543035.1:c.1668-111A= XP_011541337.1:n.1668-111A=
XM_011543035.2:c.1668-111A= XP_011541337.1:n.1668-111A=
NM_032725.4:c.1767-111A= MANE Select NP_116114.1:n.1767-111A=
NM_001159736.2:c.1365-111A= NP_001153208.1:n.1365-111A=