Canonical Allele Identifier: CA476866905
Gene: BUD13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116619222G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748506G>A , CM000673.2:g.116748506G>A GRCh38
NC_000011.9:g.116619222G>A , CM000673.1:g.116619222G>A GRCh37
NC_000011.8:g.116124432G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1836C>T MANE Select ENSP00000260210.3:p.Tyr612=
ENST00000260210.4:c.1836C>T ENSP00000260210.3:p.Tyr612=
ENST00000375445.7:c.1434C>T ENSP00000364594.3:p.Tyr478=
ENST00000419189.1:c.611C>T
NM_001159736.1:c.1434C>T NP_001153208.1:p.Tyr478=
NM_032725.3:c.1836C>T NP_116114.1:p.Tyr612=
XM_011543035.1:c.1737C>T XP_011541337.1:p.Tyr579=
XM_011543035.2:c.1737C>T XP_011541337.1:p.Tyr579=
NM_032725.4:c.1836C>T MANE Select NP_116114.1:p.Tyr612=
NM_001159736.2:c.1434C>T NP_001153208.1:p.Tyr478=