Canonical Allele Identifier: CA2002715480

Gene: BUD13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116755749_116755753delinsGTAAT , CM000673.2:g.116755749_116755753delinsGTAAT	GRCh38
NC_000011.9:g.116626465_116626469delinsGTAAT , CM000673.1:g.116626465_116626469delinsGTAAT	GRCh37
NC_000011.8:g.116131675_116131679delinsGTAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1766+1393_1766+1397delinsATTAC MANE Select	ENSP00000260210.3:n.1766+1393_1766+1397delinsATTAC
ENST00000260210.4:c.1766+1393_1766+1397delinsATTAC	ENSP00000260210.3:n.1766+1393_1766+1397delinsATTAC
ENST00000375445.7:c.1364+1393_1364+1397delinsATTAC	ENSP00000364594.3:n.1364+1393_1364+1397delinsATTAC
ENST00000419189.1:c.541+1393_541+1397delinsATTAC
NM_001159736.1:c.1364+1393_1364+1397delinsATTAC	NP_001153208.1:n.1364+1393_1364+1397delinsATTAC
NM_032725.3:c.1766+1393_1766+1397delinsATTAC	NP_116114.1:n.1766+1393_1766+1397delinsATTAC
XM_011543035.1:c.1667+1393_1667+1397delinsATTAC	XP_011541337.1:n.1667+1393_1667+1397delinsATTAC
XM_011543035.2:c.1667+1393_1667+1397delinsATTAC	XP_011541337.1:n.1667+1393_1667+1397delinsATTAC
NM_032725.4:c.1766+1393_1766+1397delinsATTAC MANE Select	NP_116114.1:n.1766+1393_1766+1397delinsATTAC
NM_001159736.2:c.1364+1393_1364+1397delinsATTAC	NP_001153208.1:n.1364+1393_1364+1397delinsATTAC