Canonical Allele Identifier: CA2002715210

Gene: BUD13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116755559_116755560delinsCA , CM000673.2:g.116755559_116755560delinsCA	GRCh38
NC_000011.9:g.116626275_116626276delinsCA , CM000673.1:g.116626275_116626276delinsCA	GRCh37
NC_000011.8:g.116131485_116131486delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1766+1586_1766+1587delinsTG MANE Select	ENSP00000260210.3:n.1766+1586_1766+1587delinsTG
ENST00000260210.4:c.1766+1586_1766+1587delinsTG	ENSP00000260210.3:n.1766+1586_1766+1587delinsTG
ENST00000375445.7:c.1364+1586_1364+1587delinsTG	ENSP00000364594.3:n.1364+1586_1364+1587delinsTG
ENST00000419189.1:c.541+1586_541+1587delinsTG
NM_001159736.1:c.1364+1586_1364+1587delinsTG	NP_001153208.1:n.1364+1586_1364+1587delinsTG
NM_032725.3:c.1766+1586_1766+1587delinsTG	NP_116114.1:n.1766+1586_1766+1587delinsTG
XM_011543035.1:c.1667+1586_1667+1587delinsTG	XP_011541337.1:n.1667+1586_1667+1587delinsTG
XM_011543035.2:c.1667+1586_1667+1587delinsTG	XP_011541337.1:n.1667+1586_1667+1587delinsTG
NM_032725.4:c.1766+1586_1766+1587delinsTG MANE Select	NP_116114.1:n.1766+1586_1766+1587delinsTG
NM_001159736.2:c.1364+1586_1364+1587delinsTG	NP_001153208.1:n.1364+1586_1364+1587delinsTG