Canonical Allele Identifier: CA2002715342

Gene: BUD13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116755657_116755659delinsCAG , CM000673.2:g.116755657_116755659delinsCAG	GRCh38
NC_000011.9:g.116626373_116626375delinsCAG , CM000673.1:g.116626373_116626375delinsCAG	GRCh37
NC_000011.8:g.116131583_116131585delinsCAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1766+1487_1766+1489delinsCTG MANE Select	ENSP00000260210.3:n.1766+1487_1766+1489delinsCTG
ENST00000260210.4:c.1766+1487_1766+1489delinsCTG	ENSP00000260210.3:n.1766+1487_1766+1489delinsCTG
ENST00000375445.7:c.1364+1487_1364+1489delinsCTG	ENSP00000364594.3:n.1364+1487_1364+1489delinsCTG
ENST00000419189.1:c.541+1487_541+1489delinsCTG
NM_001159736.1:c.1364+1487_1364+1489delinsCTG	NP_001153208.1:n.1364+1487_1364+1489delinsCTG
NM_032725.3:c.1766+1487_1766+1489delinsCTG	NP_116114.1:n.1766+1487_1766+1489delinsCTG
XM_011543035.1:c.1667+1487_1667+1489delinsCTG	XP_011541337.1:n.1667+1487_1667+1489delinsCTG
XM_011543035.2:c.1667+1487_1667+1489delinsCTG	XP_011541337.1:n.1667+1487_1667+1489delinsCTG
NM_032725.4:c.1766+1487_1766+1489delinsCTG MANE Select	NP_116114.1:n.1766+1487_1766+1489delinsCTG
NM_001159736.2:c.1364+1487_1364+1489delinsCTG	NP_001153208.1:n.1364+1487_1364+1489delinsCTG