Canonical Allele Identifier: CA2002706454

Gene: BUD13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116748797_116748805delinsCTAATATGG , CM000673.2:g.116748797_116748805delinsCTAATATGG	GRCh38
NC_000011.9:g.116619513_116619521delinsCTAATATGG , CM000673.1:g.116619513_116619521delinsCTAATATGG	GRCh37
NC_000011.8:g.116124723_116124731delinsCTAATATGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1767-230_1767-222delinsCCATATTAG MANE Select	ENSP00000260210.3:n.1767-230_1767-222delinsCCATATTAG
ENST00000260210.4:c.1767-230_1767-222delinsCCATATTAG	ENSP00000260210.3:n.1767-230_1767-222delinsCCATATTAG
ENST00000375445.7:c.1365-230_1365-222delinsCCATATTAG	ENSP00000364594.3:n.1365-230_1365-222delinsCCATATTAG
ENST00000419189.1:c.542-230_542-222delinsCCATATTAG
NM_001159736.1:c.1365-230_1365-222delinsCCATATTAG	NP_001153208.1:n.1365-230_1365-222delinsCCATATTAG
NM_032725.3:c.1767-230_1767-222delinsCCATATTAG	NP_116114.1:n.1767-230_1767-222delinsCCATATTAG
XM_011543035.1:c.1668-230_1668-222delinsCCATATTAG	XP_011541337.1:n.1668-230_1668-222delinsCCATATTAG
XM_011543035.2:c.1668-230_1668-222delinsCCATATTAG	XP_011541337.1:n.1668-230_1668-222delinsCCATATTAG
NM_032725.4:c.1767-230_1767-222delinsCCATATTAG MANE Select	NP_116114.1:n.1767-230_1767-222delinsCCATATTAG
NM_001159736.2:c.1365-230_1365-222delinsCCATATTAG	NP_001153208.1:n.1365-230_1365-222delinsCCATATTAG