Canonical Allele Identifier: CA2002715699
Gene: BUD13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116755912_116755913delinsAT , CM000673.2:g.116755912_116755913delinsAT GRCh38
NC_000011.9:g.116626628_116626629delinsAT , CM000673.1:g.116626628_116626629delinsAT GRCh37
NC_000011.8:g.116131838_116131839delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1766+1233_1766+1234delinsAT MANE Select ENSP00000260210.3:n.1766+1233_1766+1234delinsAT
ENST00000260210.4:c.1766+1233_1766+1234delinsAT ENSP00000260210.3:n.1766+1233_1766+1234delinsAT
ENST00000375445.7:c.1364+1233_1364+1234delinsAT ENSP00000364594.3:n.1364+1233_1364+1234delinsAT
ENST00000419189.1:c.541+1233_541+1234delinsAT
NM_001159736.1:c.1364+1233_1364+1234delinsAT NP_001153208.1:n.1364+1233_1364+1234delinsAT
NM_032725.3:c.1766+1233_1766+1234delinsAT NP_116114.1:n.1766+1233_1766+1234delinsAT
XM_011543035.1:c.1667+1233_1667+1234delinsAT XP_011541337.1:n.1667+1233_1667+1234delinsAT
XM_011543035.2:c.1667+1233_1667+1234delinsAT XP_011541337.1:n.1667+1233_1667+1234delinsAT
NM_032725.4:c.1766+1233_1766+1234delinsAT MANE Select NP_116114.1:n.1766+1233_1766+1234delinsAT
NM_001159736.2:c.1364+1233_1364+1234delinsAT NP_001153208.1:n.1364+1233_1364+1234delinsAT