Canonical Allele Identifier: CA382695170
Gene: BUD13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748533G>C , CM000673.2:g.116748533G>C GRCh38
NC_000011.9:g.116619249G>C , CM000673.1:g.116619249G>C GRCh37
NC_000011.8:g.116124459G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1809C>G MANE Select ENSP00000260210.3:p.Ser603Arg
ENST00000260210.4:c.1809C>G ENSP00000260210.3:p.Ser603Arg
ENST00000375445.7:c.1407C>G ENSP00000364594.3:p.Ser469Arg
ENST00000419189.1:c.584C>G
NM_001159736.1:c.1407C>G NP_001153208.1:p.Ser469Arg
NM_032725.3:c.1809C>G NP_116114.1:p.Ser603Arg
XM_011543035.1:c.1710C>G XP_011541337.1:p.Ser570Arg
XM_011543035.2:c.1710C>G XP_011541337.1:p.Ser570Arg
NM_032725.4:c.1809C>G MANE Select NP_116114.1:p.Ser603Arg
NM_001159736.2:c.1407C>G NP_001153208.1:p.Ser469Arg