Canonical Allele Identifier: CA2002715528

Gene: BUD13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116755795_116755799delinsAGTTT , CM000673.2:g.116755795_116755799delinsAGTTT	GRCh38
NC_000011.9:g.116626511_116626515delinsAGTTT , CM000673.1:g.116626511_116626515delinsAGTTT	GRCh37
NC_000011.8:g.116131721_116131725delinsAGTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1766+1347_1766+1351delinsAAACT MANE Select	ENSP00000260210.3:n.1766+1347_1766+1351delinsAAACT
ENST00000260210.4:c.1766+1347_1766+1351delinsAAACT	ENSP00000260210.3:n.1766+1347_1766+1351delinsAAACT
ENST00000375445.7:c.1364+1347_1364+1351delinsAAACT	ENSP00000364594.3:n.1364+1347_1364+1351delinsAAACT
ENST00000419189.1:c.541+1347_541+1351delinsAAACT
NM_001159736.1:c.1364+1347_1364+1351delinsAAACT	NP_001153208.1:n.1364+1347_1364+1351delinsAAACT
NM_032725.3:c.1766+1347_1766+1351delinsAAACT	NP_116114.1:n.1766+1347_1766+1351delinsAAACT
XM_011543035.1:c.1667+1347_1667+1351delinsAAACT	XP_011541337.1:n.1667+1347_1667+1351delinsAAACT
XM_011543035.2:c.1667+1347_1667+1351delinsAAACT	XP_011541337.1:n.1667+1347_1667+1351delinsAAACT
NM_032725.4:c.1766+1347_1766+1351delinsAAACT MANE Select	NP_116114.1:n.1766+1347_1766+1351delinsAAACT
NM_001159736.2:c.1364+1347_1364+1351delinsAAACT	NP_001153208.1:n.1364+1347_1364+1351delinsAAACT