Canonical Allele Identifier: CA2002715541

Gene: BUD13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116755800_116755803delinsATTT , CM000673.2:g.116755800_116755803delinsATTT	GRCh38
NC_000011.9:g.116626516_116626519delinsATTT , CM000673.1:g.116626516_116626519delinsATTT	GRCh37
NC_000011.8:g.116131726_116131729delinsATTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1766+1343_1766+1346delinsAAAT MANE Select	ENSP00000260210.3:n.1766+1343_1766+1346delinsAAAT
ENST00000260210.4:c.1766+1343_1766+1346delinsAAAT	ENSP00000260210.3:n.1766+1343_1766+1346delinsAAAT
ENST00000375445.7:c.1364+1343_1364+1346delinsAAAT	ENSP00000364594.3:n.1364+1343_1364+1346delinsAAAT
ENST00000419189.1:c.541+1343_541+1346delinsAAAT
NM_001159736.1:c.1364+1343_1364+1346delinsAAAT	NP_001153208.1:n.1364+1343_1364+1346delinsAAAT
NM_032725.3:c.1766+1343_1766+1346delinsAAAT	NP_116114.1:n.1766+1343_1766+1346delinsAAAT
XM_011543035.1:c.1667+1343_1667+1346delinsAAAT	XP_011541337.1:n.1667+1343_1667+1346delinsAAAT
XM_011543035.2:c.1667+1343_1667+1346delinsAAAT	XP_011541337.1:n.1667+1343_1667+1346delinsAAAT
NM_032725.4:c.1766+1343_1766+1346delinsAAAT MANE Select	NP_116114.1:n.1766+1343_1766+1346delinsAAAT
NM_001159736.2:c.1364+1343_1364+1346delinsAAAT	NP_001153208.1:n.1364+1343_1364+1346delinsAAAT