Canonical Allele Identifier: CA2002705689
Gene: BUD13 HGNC NCBI

Linked Data

dbSNP Id: rs1940176146
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748353A>G , CM000673.2:g.116748353A>G GRCh38
NC_000011.9:g.116619069A>G , CM000673.1:g.116619069A>G GRCh37
NC_000011.8:g.116124279A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260210.5:c.*129T>C MANE Select ENSP00000260210.3:n.*129T>C
ENST00000260210.4:c.*129T>C ENSP00000260210.3:n.*129T>C
ENST00000375445.7:c.*129T>C ENSP00000364594.3:n.*129T>C
ENST00000419189.1:c.764T>C
NM_001159736.1:c.*129T>C NP_001153208.1:n.*129T>C
NM_032725.3:c.*129T>C NP_116114.1:n.*129T>C
XM_011543035.1:c.*129T>C XP_011541337.1:n.*129T>C
XM_011543035.2:c.*129T>C XP_011541337.1:n.*129T>C
NM_032725.4:c.*129T>C MANE Select NP_116114.1:n.*129T>C
NM_001159736.2:c.*129T>C NP_001153208.1:n.*129T>C
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