Canonical Allele Identifier: CA382695114
Gene: BUD13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748508A>G , CM000673.2:g.116748508A>G GRCh38
NC_000011.9:g.116619224A>G , CM000673.1:g.116619224A>G GRCh37
NC_000011.8:g.116124434A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1834T>C MANE Select ENSP00000260210.3:p.Tyr612His
ENST00000260210.4:c.1834T>C ENSP00000260210.3:p.Tyr612His
ENST00000375445.7:c.1432T>C ENSP00000364594.3:p.Tyr478His
ENST00000419189.1:c.609T>C
NM_001159736.1:c.1432T>C NP_001153208.1:p.Tyr478His
NM_032725.3:c.1834T>C NP_116114.1:p.Tyr612His
XM_011543035.1:c.1735T>C XP_011541337.1:p.Tyr579His
XM_011543035.2:c.1735T>C XP_011541337.1:p.Tyr579His
NM_032725.4:c.1834T>C MANE Select NP_116114.1:p.Tyr612His
NM_001159736.2:c.1432T>C NP_001153208.1:p.Tyr478His