Canonical Allele Identifier: CA2616107802
Gene: BUD13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748722_116748729del , CM000673.2:g.116748722_116748729del GRCh38
NC_000011.9:g.116619438_116619445del , CM000673.1:g.116619438_116619445del GRCh37
NC_000011.8:g.116124648_116124655del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1767-154_1767-147del MANE Select ENSP00000260210.3:n.1767-154_1767-147del
ENST00000260210.4:c.1767-154_1767-147del ENSP00000260210.3:n.1767-154_1767-147del
ENST00000375445.7:c.1365-154_1365-147del ENSP00000364594.3:n.1365-154_1365-147del
ENST00000419189.1:c.542-154_542-147del
NM_001159736.1:c.1365-154_1365-147del NP_001153208.1:n.1365-154_1365-147del
NM_032725.3:c.1767-154_1767-147del NP_116114.1:n.1767-154_1767-147del
XM_011543035.1:c.1668-154_1668-147del XP_011541337.1:n.1668-154_1668-147del
XM_011543035.2:c.1668-154_1668-147del XP_011541337.1:n.1668-154_1668-147del
NM_032725.4:c.1767-154_1767-147del MANE Select NP_116114.1:n.1767-154_1767-147del
NM_001159736.2:c.1365-154_1365-147del NP_001153208.1:n.1365-154_1365-147del