Canonical Allele Identifier: CA382695212
Gene: BUD13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748553G>T , CM000673.2:g.116748553G>T GRCh38
NC_000011.9:g.116619269G>T , CM000673.1:g.116619269G>T GRCh37
NC_000011.8:g.116124479G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1789C>A MANE Select ENSP00000260210.3:p.Arg597Ser
ENST00000260210.4:c.1789C>A ENSP00000260210.3:p.Arg597Ser
ENST00000375445.7:c.1387C>A ENSP00000364594.3:p.Arg463Ser
ENST00000419189.1:c.564C>A
NM_001159736.1:c.1387C>A NP_001153208.1:p.Arg463Ser
NM_032725.3:c.1789C>A NP_116114.1:p.Arg597Ser
XM_011543035.1:c.1690C>A XP_011541337.1:p.Arg564Ser
XM_011543035.2:c.1690C>A XP_011541337.1:p.Arg564Ser
NM_032725.4:c.1789C>A MANE Select NP_116114.1:p.Arg597Ser
NM_001159736.2:c.1387C>A NP_001153208.1:p.Arg463Ser