Canonical Allele Identifier: CA476866936
Gene: BUD13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116619270C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748554C>T , CM000673.2:g.116748554C>T GRCh38
NC_000011.9:g.116619270C>T , CM000673.1:g.116619270C>T GRCh37
NC_000011.8:g.116124480C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1788G>A MANE Select ENSP00000260210.3:p.Lys596=
ENST00000260210.4:c.1788G>A ENSP00000260210.3:p.Lys596=
ENST00000375445.7:c.1386G>A ENSP00000364594.3:p.Lys462=
ENST00000419189.1:c.563G>A
NM_001159736.1:c.1386G>A NP_001153208.1:p.Lys462=
NM_032725.3:c.1788G>A NP_116114.1:p.Lys596=
XM_011543035.1:c.1689G>A XP_011541337.1:p.Lys563=
XM_011543035.2:c.1689G>A XP_011541337.1:p.Lys563=
NM_032725.4:c.1788G>A MANE Select NP_116114.1:p.Lys596=
NM_001159736.2:c.1386G>A NP_001153208.1:p.Lys462=