Canonical Allele Identifier: CA476866900

Gene: BUD13

Linked Data

• MyVariant Identifiers: chr11:g.116619204A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116748488A>G , CM000673.2:g.116748488A>G	GRCh38
NC_000011.9:g.116619204A>G , CM000673.1:g.116619204A>G	GRCh37
NC_000011.8:g.116124414A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1854T>C MANE Select	ENSP00000260210.3:p.Asp618=
ENST00000260210.4:c.1854T>C	ENSP00000260210.3:p.Asp618=
ENST00000375445.7:c.1452T>C	ENSP00000364594.3:p.Asp484=
ENST00000419189.1:c.629T>C
NM_001159736.1:c.1452T>C	NP_001153208.1:p.Asp484=
NM_032725.3:c.1854T>C	NP_116114.1:p.Asp618=
XM_011543035.1:c.1755T>C	XP_011541337.1:p.Asp585=
XM_011543035.2:c.1755T>C	XP_011541337.1:p.Asp585=
NM_032725.4:c.1854T>C MANE Select	NP_116114.1:p.Asp618=
NM_001159736.2:c.1452T>C	NP_001153208.1:p.Asp484=