Canonical Allele Identifier: CA2002715525

Gene: BUD13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116755792_116755797delinsATTAGT , CM000673.2:g.116755792_116755797delinsATTAGT	GRCh38
NC_000011.9:g.116626508_116626513delinsATTAGT , CM000673.1:g.116626508_116626513delinsATTAGT	GRCh37
NC_000011.8:g.116131718_116131723delinsATTAGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1766+1349_1766+1354delinsACTAAT MANE Select	ENSP00000260210.3:n.1766+1349_1766+1354delinsACTAAT
ENST00000260210.4:c.1766+1349_1766+1354delinsACTAAT	ENSP00000260210.3:n.1766+1349_1766+1354delinsACTAAT
ENST00000375445.7:c.1364+1349_1364+1354delinsACTAAT	ENSP00000364594.3:n.1364+1349_1364+1354delinsACTAAT
ENST00000419189.1:c.541+1349_541+1354delinsACTAAT
NM_001159736.1:c.1364+1349_1364+1354delinsACTAAT	NP_001153208.1:n.1364+1349_1364+1354delinsACTAAT
NM_032725.3:c.1766+1349_1766+1354delinsACTAAT	NP_116114.1:n.1766+1349_1766+1354delinsACTAAT
XM_011543035.1:c.1667+1349_1667+1354delinsACTAAT	XP_011541337.1:n.1667+1349_1667+1354delinsACTAAT
XM_011543035.2:c.1667+1349_1667+1354delinsACTAAT	XP_011541337.1:n.1667+1349_1667+1354delinsACTAAT
NM_032725.4:c.1766+1349_1766+1354delinsACTAAT MANE Select	NP_116114.1:n.1766+1349_1766+1354delinsACTAAT
NM_001159736.2:c.1364+1349_1364+1354delinsACTAAT	NP_001153208.1:n.1364+1349_1364+1354delinsACTAAT