Canonical Allele Identifier: CA2002705972
Gene: BUD13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748497A= , CM000673.2:g.116748497A= GRCh38
NC_000011.9:g.116619213A= , CM000673.1:g.116619213A= GRCh37
NC_000011.8:g.116124423A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.1845T= MANE Select ENSP00000260210.3:p.Ser615=
ENST00000260210.4:c.1845T= ENSP00000260210.3:p.Ser615=
ENST00000375445.7:c.1443T= ENSP00000364594.3:p.Ser481=
ENST00000419189.1:c.620T=
NM_001159736.1:c.1443T= NP_001153208.1:p.Ser481=
NM_032725.3:c.1845T= NP_116114.1:p.Ser615=
XM_011543035.1:c.1746T= XP_011541337.1:p.Ser582=
XM_011543035.2:c.1746T= XP_011541337.1:p.Ser582=
NM_032725.4:c.1845T= MANE Select NP_116114.1:p.Ser615=
NM_001159736.2:c.1443T= NP_001153208.1:p.Ser481=