Canonical Allele Identifier: CA2002705453
Gene: BUD13 HGNC NCBI

Linked Data

dbSNP Id: rs1431961570

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748206dup , CM000673.2:g.116748206dup GRCh38
NC_000011.9:g.116618922dup , CM000673.1:g.116618922dup GRCh37
NC_000011.8:g.116124132dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.*281dup MANE Select ENSP00000260210.3:n.*281dup
ENST00000260210.4:c.*281dup ENSP00000260210.3:n.*281dup
ENST00000375445.7:c.*281dup ENSP00000364594.3:n.*281dup
ENST00000419189.1:c.916dup
NM_001159736.1:c.*281dup NP_001153208.1:n.*281dup
NM_032725.3:c.*281dup NP_116114.1:n.*281dup
XM_011543035.1:c.*281dup XP_011541337.1:n.*281dup
XM_011543035.2:c.*281dup XP_011541337.1:n.*281dup
NM_032725.4:c.*281dup MANE Select NP_116114.1:n.*281dup
NM_001159736.2:c.*281dup NP_001153208.1:n.*281dup