Canonical Allele Identifier: CA476866942

Gene: BUD13

Linked Data

• MyVariant Identifiers: chr11:g.116619282T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116748566T>G , CM000673.2:g.116748566T>G	GRCh38
NC_000011.9:g.116619282T>G , CM000673.1:g.116619282T>G	GRCh37
NC_000011.8:g.116124492T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1776A>C MANE Select	ENSP00000260210.3:p.Gly592=
ENST00000260210.4:c.1776A>C	ENSP00000260210.3:p.Gly592=
ENST00000375445.7:c.1374A>C	ENSP00000364594.3:p.Gly458=
ENST00000419189.1:c.551A>C
NM_001159736.1:c.1374A>C	NP_001153208.1:p.Gly458=
NM_032725.3:c.1776A>C	NP_116114.1:p.Gly592=
XM_011543035.1:c.1677A>C	XP_011541337.1:p.Gly559=
XM_011543035.2:c.1677A>C	XP_011541337.1:p.Gly559=
NM_032725.4:c.1776A>C MANE Select	NP_116114.1:p.Gly592=
NM_001159736.2:c.1374A>C	NP_001153208.1:p.Gly458=