Canonical Allele Identifier: CA2002715664

Gene: BUD13

Linked Data

• dbSNP Id: rs1940314146

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116755887del , CM000673.2:g.116755887del	GRCh38
NC_000011.9:g.116626603del , CM000673.1:g.116626603del	GRCh37
NC_000011.8:g.116131813del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1766+1259del MANE Select	ENSP00000260210.3:n.1766+1259del
ENST00000260210.4:c.1766+1259del	ENSP00000260210.3:n.1766+1259del
ENST00000375445.7:c.1364+1259del	ENSP00000364594.3:n.1364+1259del
ENST00000419189.1:c.541+1259del
NM_001159736.1:c.1364+1259del	NP_001153208.1:n.1364+1259del
NM_032725.3:c.1766+1259del	NP_116114.1:n.1766+1259del
XM_011543035.1:c.1667+1259del	XP_011541337.1:n.1667+1259del
XM_011543035.2:c.1667+1259del	XP_011541337.1:n.1667+1259del
NM_032725.4:c.1766+1259del MANE Select	NP_116114.1:n.1766+1259del
NM_001159736.2:c.1364+1259del	NP_001153208.1:n.1364+1259del