Canonical Allele Identifier: CA2002706391
Gene: BUD13 HGNC NCBI

Linked Data

dbSNP Id: rs1940182596

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748761del , CM000673.2:g.116748761del GRCh38
NC_000011.9:g.116619477del , CM000673.1:g.116619477del GRCh37
NC_000011.8:g.116124687del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1767-184del MANE Select ENSP00000260210.3:n.1767-184del
ENST00000260210.4:c.1767-184del ENSP00000260210.3:n.1767-184del
ENST00000375445.7:c.1365-184del ENSP00000364594.3:n.1365-184del
ENST00000419189.1:c.542-184del
NM_001159736.1:c.1365-184del NP_001153208.1:n.1365-184del
NM_032725.3:c.1767-184del NP_116114.1:n.1767-184del
XM_011543035.1:c.1668-184del XP_011541337.1:n.1668-184del
XM_011543035.2:c.1668-184del XP_011541337.1:n.1668-184del
NM_032725.4:c.1767-184del MANE Select NP_116114.1:n.1767-184del
NM_001159736.2:c.1365-184del NP_001153208.1:n.1365-184del