Canonical Allele Identifier: CA2002715533
Gene: BUD13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116755799_116755800delinsTA , CM000673.2:g.116755799_116755800delinsTA GRCh38
NC_000011.9:g.116626515_116626516delinsTA , CM000673.1:g.116626515_116626516delinsTA GRCh37
NC_000011.8:g.116131725_116131726delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1766+1346_1766+1347delinsTA MANE Select ENSP00000260210.3:n.1766+1346_1766+1347delinsTA
ENST00000260210.4:c.1766+1346_1766+1347delinsTA ENSP00000260210.3:n.1766+1346_1766+1347delinsTA
ENST00000375445.7:c.1364+1346_1364+1347delinsTA ENSP00000364594.3:n.1364+1346_1364+1347delinsTA
ENST00000419189.1:c.541+1346_541+1347delinsTA
NM_001159736.1:c.1364+1346_1364+1347delinsTA NP_001153208.1:n.1364+1346_1364+1347delinsTA
NM_032725.3:c.1766+1346_1766+1347delinsTA NP_116114.1:n.1766+1346_1766+1347delinsTA
XM_011543035.1:c.1667+1346_1667+1347delinsTA XP_011541337.1:n.1667+1346_1667+1347delinsTA
XM_011543035.2:c.1667+1346_1667+1347delinsTA XP_011541337.1:n.1667+1346_1667+1347delinsTA
NM_032725.4:c.1766+1346_1766+1347delinsTA MANE Select NP_116114.1:n.1766+1346_1766+1347delinsTA
NM_001159736.2:c.1364+1346_1364+1347delinsTA NP_001153208.1:n.1364+1346_1364+1347delinsTA