Canonical Allele Identifier: CA224356
Gene: BCKDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 96616
ClinVar RCV Id: RCV001240186
dbSNP Id: rs398124599

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80203146del , CM000668.2:g.80203146del GRCh38
NC_000006.11:g.80912863del , CM000668.1:g.80912863del GRCh37
NC_000006.10:g.80969582del NCBI36
NG_009775.1:g.101520del
NG_009775.2:g.101520del

Transcript Alleles

HGVS Amino-acid change
ENST00000320393.9:c.885del MANE Select ENSP00000318351.5:p.Gly296GlufsTer9
ENST00000320393.8:c.885del ENSP00000318351.5:p.Gly296GlufsTer9
ENST00000356489.9:c.885del ENSP00000348880.5:p.Gly296GlufsTer9
ENST00000468520.1:n.45del
NM_000056.3:c.885del NP_000047.1:p.Gly296GlufsTer9
NM_183050.2:c.885del NP_898871.1:p.Gly296GlufsTer9
XM_005248756.3:c.885del XP_005248813.1:p.Gly296GlufsTer9
XM_006715542.2:c.675del XP_006715605.1:p.Gly226GlufsTer9
XM_011536023.1:c.885del XP_011534325.1:p.Gly296GlufsTer9
XM_011536024.1:c.885del XP_011534326.1:p.Gly296GlufsTer9
XM_011536025.1:c.885del XP_011534327.1:p.Gly296GlufsTer9
XM_011536026.1:c.675del XP_011534328.1:p.Gly226GlufsTer9
NM_000056.4:c.885del NP_000047.1:p.Gly296GlufsTer9
NM_001318975.1:c.675del NP_001305904.1:p.Gly226GlufsTer9
NM_183050.3:c.885del NP_898871.1:p.Gly296GlufsTer9
NR_134945.1:n.1063del
XM_005248756.5:c.885del XP_005248813.1:p.Gly296GlufsTer9
XM_011536023.3:c.885del XP_011534325.1:p.Gly296GlufsTer9
XM_011536024.3:c.885del XP_011534326.1:p.Gly296GlufsTer9
XM_011536025.3:c.885del XP_011534327.1:p.Gly296GlufsTer9
XR_001743546.2:n.915del
XR_001743547.2:n.915del
XR_001743548.2:n.915del
XR_001743549.2:n.915del
XR_002956292.1:n.915del
NM_183050.4:c.885del MANE Select NP_898871.1:p.Gly296GlufsTer9
NR_134945.2:n.1002del
NM_000056.5:c.885del NP_000047.1:p.Gly296GlufsTer9