Canonical Allele Identifier: CA2002705604
Gene: BUD13 HGNC NCBI

Linked Data

dbSNP Id: rs1940175114

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748304_116748305insGTG , CM000673.2:g.116748304_116748305insGTG GRCh38
NC_000011.9:g.116619020_116619021insGTG , CM000673.1:g.116619020_116619021insGTG GRCh37
NC_000011.8:g.116124230_116124231insGTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260210.5:c.*177_*178insCAC MANE Select ENSP00000260210.3:n.*177_*178insCAC
ENST00000260210.4:c.*177_*178insCAC ENSP00000260210.3:n.*177_*178insCAC
ENST00000375445.7:c.*177_*178insCAC ENSP00000364594.3:n.*177_*178insCAC
ENST00000419189.1:c.812_813insCAC
NM_001159736.1:c.*177_*178insCAC NP_001153208.1:n.*177_*178insCAC
NM_032725.3:c.*177_*178insCAC NP_116114.1:n.*177_*178insCAC
XM_011543035.1:c.*177_*178insCAC XP_011541337.1:n.*177_*178insCAC
XM_011543035.2:c.*177_*178insCAC XP_011541337.1:n.*177_*178insCAC
NM_032725.4:c.*177_*178insCAC MANE Select NP_116114.1:n.*177_*178insCAC
NM_001159736.2:c.*177_*178insCAC NP_001153208.1:n.*177_*178insCAC