Canonical Allele Identifier: CA382695142
Gene: BUD13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748522A>C , CM000673.2:g.116748522A>C GRCh38
NC_000011.9:g.116619238A>C , CM000673.1:g.116619238A>C GRCh37
NC_000011.8:g.116124448A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1820T>G MANE Select ENSP00000260210.3:p.Val607Gly
ENST00000260210.4:c.1820T>G ENSP00000260210.3:p.Val607Gly
ENST00000375445.7:c.1418T>G ENSP00000364594.3:p.Val473Gly
ENST00000419189.1:c.595T>G
NM_001159736.1:c.1418T>G NP_001153208.1:p.Val473Gly
NM_032725.3:c.1820T>G NP_116114.1:p.Val607Gly
XM_011543035.1:c.1721T>G XP_011541337.1:p.Val574Gly
XM_011543035.2:c.1721T>G XP_011541337.1:p.Val574Gly
NM_032725.4:c.1820T>G MANE Select NP_116114.1:p.Val607Gly
NM_001159736.2:c.1418T>G NP_001153208.1:p.Val473Gly