Canonical Allele Identifier: CA2002715374

Gene: BUD13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116755671_116755674delinsCTAT , CM000673.2:g.116755671_116755674delinsCTAT	GRCh38
NC_000011.9:g.116626387_116626390delinsCTAT , CM000673.1:g.116626387_116626390delinsCTAT	GRCh37
NC_000011.8:g.116131597_116131600delinsCTAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1766+1472_1766+1475delinsATAG MANE Select	ENSP00000260210.3:n.1766+1472_1766+1475delinsATAG
ENST00000260210.4:c.1766+1472_1766+1475delinsATAG	ENSP00000260210.3:n.1766+1472_1766+1475delinsATAG
ENST00000375445.7:c.1364+1472_1364+1475delinsATAG	ENSP00000364594.3:n.1364+1472_1364+1475delinsATAG
ENST00000419189.1:c.541+1472_541+1475delinsATAG
NM_001159736.1:c.1364+1472_1364+1475delinsATAG	NP_001153208.1:n.1364+1472_1364+1475delinsATAG
NM_032725.3:c.1766+1472_1766+1475delinsATAG	NP_116114.1:n.1766+1472_1766+1475delinsATAG
XM_011543035.1:c.1667+1472_1667+1475delinsATAG	XP_011541337.1:n.1667+1472_1667+1475delinsATAG
XM_011543035.2:c.1667+1472_1667+1475delinsATAG	XP_011541337.1:n.1667+1472_1667+1475delinsATAG
NM_032725.4:c.1766+1472_1766+1475delinsATAG MANE Select	NP_116114.1:n.1766+1472_1766+1475delinsATAG
NM_001159736.2:c.1364+1472_1364+1475delinsATAG	NP_001153208.1:n.1364+1472_1364+1475delinsATAG