Canonical Allele Identifier: CA2002705999
Gene: BUD13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748527C= , CM000673.2:g.116748527C= GRCh38
NC_000011.9:g.116619243C= , CM000673.1:g.116619243C= GRCh37
NC_000011.8:g.116124453C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1815G= MANE Select ENSP00000260210.3:p.Lys605=
ENST00000260210.4:c.1815G= ENSP00000260210.3:p.Lys605=
ENST00000375445.7:c.1413G= ENSP00000364594.3:p.Lys471=
ENST00000419189.1:c.590G=
NM_001159736.1:c.1413G= NP_001153208.1:p.Lys471=
NM_032725.3:c.1815G= NP_116114.1:p.Lys605=
XM_011543035.1:c.1716G= XP_011541337.1:p.Lys572=
XM_011543035.2:c.1716G= XP_011541337.1:p.Lys572=
NM_032725.4:c.1815G= MANE Select NP_116114.1:p.Lys605=
NM_001159736.2:c.1413G= NP_001153208.1:p.Lys471=