Canonical Allele Identifier: CA2725022169
Gene: BUD13 HGNC NCBI

Linked Data

dbSNP Id: rs2134173433

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116755479_116755482del , CM000673.2:g.116755479_116755482del GRCh38
NC_000011.9:g.116626195_116626198del , CM000673.1:g.116626195_116626198del GRCh37
NC_000011.8:g.116131405_116131408del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260210.5:c.1766+1666_1766+1669del MANE Select ENSP00000260210.3:n.1766+1666_1766+1669del
ENST00000260210.4:c.1766+1666_1766+1669del ENSP00000260210.3:n.1766+1666_1766+1669del
ENST00000375445.7:c.1364+1666_1364+1669del ENSP00000364594.3:n.1364+1666_1364+1669del
ENST00000419189.1:c.541+1666_541+1669del
NM_001159736.1:c.1364+1666_1364+1669del NP_001153208.1:n.1364+1666_1364+1669del
NM_032725.3:c.1766+1666_1766+1669del NP_116114.1:n.1766+1666_1766+1669del
XM_011543035.1:c.1667+1666_1667+1669del XP_011541337.1:n.1667+1666_1667+1669del
XM_011543035.2:c.1667+1666_1667+1669del XP_011541337.1:n.1667+1666_1667+1669del
NM_032725.4:c.1766+1666_1766+1669del MANE Select NP_116114.1:n.1766+1666_1766+1669del
NM_001159736.2:c.1364+1666_1364+1669del NP_001153208.1:n.1364+1666_1364+1669del