Canonical Allele Identifier: CA2002715519

Gene: BUD13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116755788_116755794delinsCATAATT , CM000673.2:g.116755788_116755794delinsCATAATT	GRCh38
NC_000011.9:g.116626504_116626510delinsCATAATT , CM000673.1:g.116626504_116626510delinsCATAATT	GRCh37
NC_000011.8:g.116131714_116131720delinsCATAATT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1766+1352_1766+1358delinsAATTATG MANE Select	ENSP00000260210.3:n.1766+1352_1766+1358delinsAATTATG
ENST00000260210.4:c.1766+1352_1766+1358delinsAATTATG	ENSP00000260210.3:n.1766+1352_1766+1358delinsAATTATG
ENST00000375445.7:c.1364+1352_1364+1358delinsAATTATG	ENSP00000364594.3:n.1364+1352_1364+1358delinsAATTATG
ENST00000419189.1:c.541+1352_541+1358delinsAATTATG
NM_001159736.1:c.1364+1352_1364+1358delinsAATTATG	NP_001153208.1:n.1364+1352_1364+1358delinsAATTATG
NM_032725.3:c.1766+1352_1766+1358delinsAATTATG	NP_116114.1:n.1766+1352_1766+1358delinsAATTATG
XM_011543035.1:c.1667+1352_1667+1358delinsAATTATG	XP_011541337.1:n.1667+1352_1667+1358delinsAATTATG
XM_011543035.2:c.1667+1352_1667+1358delinsAATTATG	XP_011541337.1:n.1667+1352_1667+1358delinsAATTATG
NM_032725.4:c.1766+1352_1766+1358delinsAATTATG MANE Select	NP_116114.1:n.1766+1352_1766+1358delinsAATTATG
NM_001159736.2:c.1364+1352_1364+1358delinsAATTATG	NP_001153208.1:n.1364+1352_1364+1358delinsAATTATG