Canonical Allele Identifier: CA2002706059
Gene: BUD13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748572G= , CM000673.2:g.116748572G= GRCh38
NC_000011.9:g.116619288G= , CM000673.1:g.116619288G= GRCh37
NC_000011.8:g.116124498G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1770C= MANE Select ENSP00000260210.3:p.Ser590=
ENST00000260210.4:c.1770C= ENSP00000260210.3:p.Ser590=
ENST00000375445.7:c.1368C= ENSP00000364594.3:p.Ser456=
ENST00000419189.1:c.545C=
NM_001159736.1:c.1368C= NP_001153208.1:p.Ser456=
NM_032725.3:c.1770C= NP_116114.1:p.Ser590=
XM_011543035.1:c.1671C= XP_011541337.1:p.Ser557=
XM_011543035.2:c.1671C= XP_011541337.1:p.Ser557=
NM_032725.4:c.1770C= MANE Select NP_116114.1:p.Ser590=
NM_001159736.2:c.1368C= NP_001153208.1:p.Ser456=