Canonical Allele Identifier: CA2002706347
Gene: BUD13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748734_116748735delinsTC , CM000673.2:g.116748734_116748735delinsTC GRCh38
NC_000011.9:g.116619450_116619451delinsTC , CM000673.1:g.116619450_116619451delinsTC GRCh37
NC_000011.8:g.116124660_116124661delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1767-160_1767-159delinsGA MANE Select ENSP00000260210.3:n.1767-160_1767-159delinsGA
ENST00000260210.4:c.1767-160_1767-159delinsGA ENSP00000260210.3:n.1767-160_1767-159delinsGA
ENST00000375445.7:c.1365-160_1365-159delinsGA ENSP00000364594.3:n.1365-160_1365-159delinsGA
ENST00000419189.1:c.542-160_542-159delinsGA
NM_001159736.1:c.1365-160_1365-159delinsGA NP_001153208.1:n.1365-160_1365-159delinsGA
NM_032725.3:c.1767-160_1767-159delinsGA NP_116114.1:n.1767-160_1767-159delinsGA
XM_011543035.1:c.1668-160_1668-159delinsGA XP_011541337.1:n.1668-160_1668-159delinsGA
XM_011543035.2:c.1668-160_1668-159delinsGA XP_011541337.1:n.1668-160_1668-159delinsGA
NM_032725.4:c.1767-160_1767-159delinsGA MANE Select NP_116114.1:n.1767-160_1767-159delinsGA
NM_001159736.2:c.1365-160_1365-159delinsGA NP_001153208.1:n.1365-160_1365-159delinsGA