Canonical Allele Identifier: CA672225350
Gene: BUD13 HGNC NCBI

Linked Data

dbSNP Id: rs1424732444
MyVariant Identifiers: chr11:g.116619012C>T (hg19) chr11:g.116748296C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748296C>T , CM000673.2:g.116748296C>T GRCh38
NC_000011.9:g.116619012C>T , CM000673.1:g.116619012C>T GRCh37
NC_000011.8:g.116124222C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.*186G>A MANE Select ENSP00000260210.3:n.*186G>A
ENST00000260210.4:c.*186G>A ENSP00000260210.3:n.*186G>A
ENST00000375445.7:c.*186G>A ENSP00000364594.3:n.*186G>A
ENST00000419189.1:c.821G>A
NM_001159736.1:c.*186G>A NP_001153208.1:n.*186G>A
NM_032725.3:c.*186G>A NP_116114.1:n.*186G>A
XM_011543035.1:c.*186G>A XP_011541337.1:n.*186G>A
XM_011543035.2:c.*186G>A XP_011541337.1:n.*186G>A
NM_032725.4:c.*186G>A MANE Select NP_116114.1:n.*186G>A
NM_001159736.2:c.*186G>A NP_001153208.1:n.*186G>A
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