Canonical Allele Identifier: CA229294364

Gene: BUD13

Linked Data

• dbSNP Id: rs34413943
• MyVariant Identifiers: chr11:g.116619474_116619475insT (hg19) ; chr11:g.116748758_116748759insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116748758_116748759insT , CM000673.2:g.116748758_116748759insT	GRCh38
NC_000011.9:g.116619474_116619475insT , CM000673.1:g.116619474_116619475insT	GRCh37
NC_000011.8:g.116124684_116124685insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1767-184_1767-183insA MANE Select	ENSP00000260210.3:n.1767-184_1767-183insA
ENST00000260210.4:c.1767-184_1767-183insA	ENSP00000260210.3:n.1767-184_1767-183insA
ENST00000375445.7:c.1365-184_1365-183insA	ENSP00000364594.3:n.1365-184_1365-183insA
ENST00000419189.1:c.542-184_542-183insA
NM_001159736.1:c.1365-184_1365-183insA	NP_001153208.1:n.1365-184_1365-183insA
NM_032725.3:c.1767-184_1767-183insA	NP_116114.1:n.1767-184_1767-183insA
XM_011543035.1:c.1668-184_1668-183insA	XP_011541337.1:n.1668-184_1668-183insA
XM_011543035.2:c.1668-184_1668-183insA	XP_011541337.1:n.1668-184_1668-183insA
NM_032725.4:c.1767-184_1767-183insA MANE Select	NP_116114.1:n.1767-184_1767-183insA
NM_001159736.2:c.1365-184_1365-183insA	NP_001153208.1:n.1365-184_1365-183insA