Canonical Allele Identifier: CA382695098
Gene: BUD13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748502A>C , CM000673.2:g.116748502A>C GRCh38
NC_000011.9:g.116619218A>C , CM000673.1:g.116619218A>C GRCh37
NC_000011.8:g.116124428A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1840T>G MANE Select ENSP00000260210.3:p.Trp614Gly
ENST00000260210.4:c.1840T>G ENSP00000260210.3:p.Trp614Gly
ENST00000375445.7:c.1438T>G ENSP00000364594.3:p.Trp480Gly
ENST00000419189.1:c.615T>G
NM_001159736.1:c.1438T>G NP_001153208.1:p.Trp480Gly
NM_032725.3:c.1840T>G NP_116114.1:p.Trp614Gly
XM_011543035.1:c.1741T>G XP_011541337.1:p.Trp581Gly
XM_011543035.2:c.1741T>G XP_011541337.1:p.Trp581Gly
NM_032725.4:c.1840T>G MANE Select NP_116114.1:p.Trp614Gly
NM_001159736.2:c.1438T>G NP_001153208.1:p.Trp480Gly