Canonical Allele Identifier: CA476866938

Gene: BUD13

Linked Data

• MyVariant Identifiers: chr11:g.116619276T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116748560T>C , CM000673.2:g.116748560T>C	GRCh38
NC_000011.9:g.116619276T>C , CM000673.1:g.116619276T>C	GRCh37
NC_000011.8:g.116124486T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1782A>G MANE Select	ENSP00000260210.3:p.Glu594=
ENST00000260210.4:c.1782A>G	ENSP00000260210.3:p.Glu594=
ENST00000375445.7:c.1380A>G	ENSP00000364594.3:p.Glu460=
ENST00000419189.1:c.557A>G
NM_001159736.1:c.1380A>G	NP_001153208.1:p.Glu460=
NM_032725.3:c.1782A>G	NP_116114.1:p.Glu594=
XM_011543035.1:c.1683A>G	XP_011541337.1:p.Glu561=
XM_011543035.2:c.1683A>G	XP_011541337.1:p.Glu561=
NM_032725.4:c.1782A>G MANE Select	NP_116114.1:p.Glu594=
NM_001159736.2:c.1380A>G	NP_001153208.1:p.Glu460=