Canonical Allele Identifier: CA2002715649

Gene: BUD13

Linked Data

• dbSNP Id: rs1940313849

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116755875_116755876dup , CM000673.2:g.116755875_116755876dup	GRCh38
NC_000011.9:g.116626591_116626592dup , CM000673.1:g.116626591_116626592dup	GRCh37
NC_000011.8:g.116131801_116131802dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260210.5:c.1766+1270_1766+1271dup MANE Select	ENSP00000260210.3:n.1766+1270_1766+1271dup
ENST00000260210.4:c.1766+1270_1766+1271dup	ENSP00000260210.3:n.1766+1270_1766+1271dup
ENST00000375445.7:c.1364+1270_1364+1271dup	ENSP00000364594.3:n.1364+1270_1364+1271dup
ENST00000419189.1:c.541+1270_541+1271dup
NM_001159736.1:c.1364+1270_1364+1271dup	NP_001153208.1:n.1364+1270_1364+1271dup
NM_032725.3:c.1766+1270_1766+1271dup	NP_116114.1:n.1766+1270_1766+1271dup
XM_011543035.1:c.1667+1270_1667+1271dup	XP_011541337.1:n.1667+1270_1667+1271dup
XM_011543035.2:c.1667+1270_1667+1271dup	XP_011541337.1:n.1667+1270_1667+1271dup
NM_032725.4:c.1766+1270_1766+1271dup MANE Select	NP_116114.1:n.1766+1270_1766+1271dup
NM_001159736.2:c.1364+1270_1364+1271dup	NP_001153208.1:n.1364+1270_1364+1271dup