Canonical Allele Identifier: CA2002715565

Gene: BUD13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116755814_116755818delinsGAATA , CM000673.2:g.116755814_116755818delinsGAATA	GRCh38
NC_000011.9:g.116626530_116626534delinsGAATA , CM000673.1:g.116626530_116626534delinsGAATA	GRCh37
NC_000011.8:g.116131740_116131744delinsGAATA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1766+1328_1766+1332delinsTATTC MANE Select	ENSP00000260210.3:n.1766+1328_1766+1332delinsTATTC
ENST00000260210.4:c.1766+1328_1766+1332delinsTATTC	ENSP00000260210.3:n.1766+1328_1766+1332delinsTATTC
ENST00000375445.7:c.1364+1328_1364+1332delinsTATTC	ENSP00000364594.3:n.1364+1328_1364+1332delinsTATTC
ENST00000419189.1:c.541+1328_541+1332delinsTATTC
NM_001159736.1:c.1364+1328_1364+1332delinsTATTC	NP_001153208.1:n.1364+1328_1364+1332delinsTATTC
NM_032725.3:c.1766+1328_1766+1332delinsTATTC	NP_116114.1:n.1766+1328_1766+1332delinsTATTC
XM_011543035.1:c.1667+1328_1667+1332delinsTATTC	XP_011541337.1:n.1667+1328_1667+1332delinsTATTC
XM_011543035.2:c.1667+1328_1667+1332delinsTATTC	XP_011541337.1:n.1667+1328_1667+1332delinsTATTC
NM_032725.4:c.1766+1328_1766+1332delinsTATTC MANE Select	NP_116114.1:n.1766+1328_1766+1332delinsTATTC
NM_001159736.2:c.1364+1328_1364+1332delinsTATTC	NP_001153208.1:n.1364+1328_1364+1332delinsTATTC