Canonical Allele Identifier: CA476866915
Gene: BUD13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116619237C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748521C>A , CM000673.2:g.116748521C>A GRCh38
NC_000011.9:g.116619237C>A , CM000673.1:g.116619237C>A GRCh37
NC_000011.8:g.116124447C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1821G>T MANE Select ENSP00000260210.3:p.Val607=
ENST00000260210.4:c.1821G>T ENSP00000260210.3:p.Val607=
ENST00000375445.7:c.1419G>T ENSP00000364594.3:p.Val473=
ENST00000419189.1:c.596G>T
NM_001159736.1:c.1419G>T NP_001153208.1:p.Val473=
NM_032725.3:c.1821G>T NP_116114.1:p.Val607=
XM_011543035.1:c.1722G>T XP_011541337.1:p.Val574=
XM_011543035.2:c.1722G>T XP_011541337.1:p.Val574=
NM_032725.4:c.1821G>T MANE Select NP_116114.1:p.Val607=
NM_001159736.2:c.1419G>T NP_001153208.1:p.Val473=