Canonical Allele Identifier: CA2002715402

Gene: BUD13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116755689_116755697delinsTTAATGAGA , CM000673.2:g.116755689_116755697delinsTTAATGAGA	GRCh38
NC_000011.9:g.116626405_116626413delinsTTAATGAGA , CM000673.1:g.116626405_116626413delinsTTAATGAGA	GRCh37
NC_000011.8:g.116131615_116131623delinsTTAATGAGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1766+1449_1766+1457delinsTCTCATTAA MANE Select	ENSP00000260210.3:n.1766+1449_1766+1457delinsTCTCATTAA
ENST00000260210.4:c.1766+1449_1766+1457delinsTCTCATTAA	ENSP00000260210.3:n.1766+1449_1766+1457delinsTCTCATTAA
ENST00000375445.7:c.1364+1449_1364+1457delinsTCTCATTAA	ENSP00000364594.3:n.1364+1449_1364+1457delinsTCTCATTAA
ENST00000419189.1:c.541+1449_541+1457delinsTCTCATTAA
NM_001159736.1:c.1364+1449_1364+1457delinsTCTCATTAA	NP_001153208.1:n.1364+1449_1364+1457delinsTCTCATTAA
NM_032725.3:c.1766+1449_1766+1457delinsTCTCATTAA	NP_116114.1:n.1766+1449_1766+1457delinsTCTCATTAA
XM_011543035.1:c.1667+1449_1667+1457delinsTCTCATTAA	XP_011541337.1:n.1667+1449_1667+1457delinsTCTCATTAA
XM_011543035.2:c.1667+1449_1667+1457delinsTCTCATTAA	XP_011541337.1:n.1667+1449_1667+1457delinsTCTCATTAA
NM_032725.4:c.1766+1449_1766+1457delinsTCTCATTAA MANE Select	NP_116114.1:n.1766+1449_1766+1457delinsTCTCATTAA
NM_001159736.2:c.1364+1449_1364+1457delinsTCTCATTAA	NP_001153208.1:n.1364+1449_1364+1457delinsTCTCATTAA