Canonical Allele Identifier: CA2002715205

Gene: BUD13

Linked Data

• dbSNP Id: rs1940307576

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116755555_116755562del , CM000673.2:g.116755555_116755562del	GRCh38
NC_000011.9:g.116626271_116626278del , CM000673.1:g.116626271_116626278del	GRCh37
NC_000011.8:g.116131481_116131488del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1766+1585_1766+1592del MANE Select	ENSP00000260210.3:n.1766+1585_1766+1592del
ENST00000260210.4:c.1766+1585_1766+1592del	ENSP00000260210.3:n.1766+1585_1766+1592del
ENST00000375445.7:c.1364+1585_1364+1592del	ENSP00000364594.3:n.1364+1585_1364+1592del
ENST00000419189.1:c.541+1585_541+1592del
NM_001159736.1:c.1364+1585_1364+1592del	NP_001153208.1:n.1364+1585_1364+1592del
NM_032725.3:c.1766+1585_1766+1592del	NP_116114.1:n.1766+1585_1766+1592del
XM_011543035.1:c.1667+1585_1667+1592del	XP_011541337.1:n.1667+1585_1667+1592del
XM_011543035.2:c.1667+1585_1667+1592del	XP_011541337.1:n.1667+1585_1667+1592del
NM_032725.4:c.1766+1585_1766+1592del MANE Select	NP_116114.1:n.1766+1585_1766+1592del
NM_001159736.2:c.1364+1585_1364+1592del	NP_001153208.1:n.1364+1585_1364+1592del