Canonical Allele Identifier: CA382695258
Gene: BUD13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748573G>A , CM000673.2:g.116748573G>A GRCh38
NC_000011.9:g.116619289G>A , CM000673.1:g.116619289G>A GRCh37
NC_000011.8:g.116124499G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1769C>T MANE Select ENSP00000260210.3:p.Ser590Phe
ENST00000260210.4:c.1769C>T ENSP00000260210.3:p.Ser590Phe
ENST00000375445.7:c.1367C>T ENSP00000364594.3:p.Ser456Phe
ENST00000419189.1:c.544C>T
NM_001159736.1:c.1367C>T NP_001153208.1:p.Ser456Phe
NM_032725.3:c.1769C>T NP_116114.1:p.Ser590Phe
XM_011543035.1:c.1670C>T XP_011541337.1:p.Ser557Phe
XM_011543035.2:c.1670C>T XP_011541337.1:p.Ser557Phe
NM_032725.4:c.1769C>T MANE Select NP_116114.1:p.Ser590Phe
NM_001159736.2:c.1367C>T NP_001153208.1:p.Ser456Phe