Canonical Allele Identifier: CA2002705731
Gene: BUD13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748385T= , CM000673.2:g.116748385T= GRCh38
NC_000011.9:g.116619101T= , CM000673.1:g.116619101T= GRCh37
NC_000011.8:g.116124311T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.*97A= MANE Select ENSP00000260210.3:n.*97A=
ENST00000260210.4:c.*97A= ENSP00000260210.3:n.*97A=
ENST00000375445.7:c.*97A= ENSP00000364594.3:n.*97A=
ENST00000419189.1:c.732A=
NM_001159736.1:c.*97A= NP_001153208.1:n.*97A=
NM_032725.3:c.*97A= NP_116114.1:n.*97A=
XM_011543035.1:c.*97A= XP_011541337.1:n.*97A=
XM_011543035.2:c.*97A= XP_011541337.1:n.*97A=
NM_032725.4:c.*97A= MANE Select NP_116114.1:n.*97A=
NM_001159736.2:c.*97A= NP_001153208.1:n.*97A=