Canonical Allele Identifier: CA2002705543
Gene: BUD13 HGNC NCBI

Linked Data

dbSNP Id: rs1940174549
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748261C>T , CM000673.2:g.116748261C>T GRCh38
NC_000011.9:g.116618977C>T , CM000673.1:g.116618977C>T GRCh37
NC_000011.8:g.116124187C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260210.5:c.*221G>A MANE Select ENSP00000260210.3:n.*221G>A
ENST00000260210.4:c.*221G>A ENSP00000260210.3:n.*221G>A
ENST00000375445.7:c.*221G>A ENSP00000364594.3:n.*221G>A
ENST00000419189.1:c.856G>A
NM_001159736.1:c.*221G>A NP_001153208.1:n.*221G>A
NM_032725.3:c.*221G>A NP_116114.1:n.*221G>A
XM_011543035.1:c.*221G>A XP_011541337.1:n.*221G>A
XM_011543035.2:c.*221G>A XP_011541337.1:n.*221G>A
NM_032725.4:c.*221G>A MANE Select NP_116114.1:n.*221G>A
NM_001159736.2:c.*221G>A NP_001153208.1:n.*221G>A
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