Canonical Allele Identifier: CA2002706248

Gene: BUD13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116748671_116748672delinsGA , CM000673.2:g.116748671_116748672delinsGA	GRCh38
NC_000011.9:g.116619387_116619388delinsGA , CM000673.1:g.116619387_116619388delinsGA	GRCh37
NC_000011.8:g.116124597_116124598delinsGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1767-97_1767-96delinsTC MANE Select	ENSP00000260210.3:n.1767-97_1767-96delinsTC
ENST00000260210.4:c.1767-97_1767-96delinsTC	ENSP00000260210.3:n.1767-97_1767-96delinsTC
ENST00000375445.7:c.1365-97_1365-96delinsTC	ENSP00000364594.3:n.1365-97_1365-96delinsTC
ENST00000419189.1:c.542-97_542-96delinsTC
NM_001159736.1:c.1365-97_1365-96delinsTC	NP_001153208.1:n.1365-97_1365-96delinsTC
NM_032725.3:c.1767-97_1767-96delinsTC	NP_116114.1:n.1767-97_1767-96delinsTC
XM_011543035.1:c.1668-97_1668-96delinsTC	XP_011541337.1:n.1668-97_1668-96delinsTC
XM_011543035.2:c.1668-97_1668-96delinsTC	XP_011541337.1:n.1668-97_1668-96delinsTC
NM_032725.4:c.1767-97_1767-96delinsTC MANE Select	NP_116114.1:n.1767-97_1767-96delinsTC
NM_001159736.2:c.1365-97_1365-96delinsTC	NP_001153208.1:n.1365-97_1365-96delinsTC