Canonical Allele Identifier: CA2002715437
Gene: BUD13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116755728_116755733delinsCTGTTT , CM000673.2:g.116755728_116755733delinsCTGTTT GRCh38
NC_000011.9:g.116626444_116626449delinsCTGTTT , CM000673.1:g.116626444_116626449delinsCTGTTT GRCh37
NC_000011.8:g.116131654_116131659delinsCTGTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1766+1413_1766+1418delinsAAACAG MANE Select ENSP00000260210.3:n.1766+1413_1766+1418delinsAAACAG
ENST00000260210.4:c.1766+1413_1766+1418delinsAAACAG ENSP00000260210.3:n.1766+1413_1766+1418delinsAAACAG
ENST00000375445.7:c.1364+1413_1364+1418delinsAAACAG ENSP00000364594.3:n.1364+1413_1364+1418delinsAAACAG
ENST00000419189.1:c.541+1413_541+1418delinsAAACAG
NM_001159736.1:c.1364+1413_1364+1418delinsAAACAG NP_001153208.1:n.1364+1413_1364+1418delinsAAACAG
NM_032725.3:c.1766+1413_1766+1418delinsAAACAG NP_116114.1:n.1766+1413_1766+1418delinsAAACAG
XM_011543035.1:c.1667+1413_1667+1418delinsAAACAG XP_011541337.1:n.1667+1413_1667+1418delinsAAACAG
XM_011543035.2:c.1667+1413_1667+1418delinsAAACAG XP_011541337.1:n.1667+1413_1667+1418delinsAAACAG
NM_032725.4:c.1766+1413_1766+1418delinsAAACAG MANE Select NP_116114.1:n.1766+1413_1766+1418delinsAAACAG
NM_001159736.2:c.1364+1413_1364+1418delinsAAACAG NP_001153208.1:n.1364+1413_1364+1418delinsAAACAG