Canonical Allele Identifier: CA915944360
Gene: BCKDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 558247
ClinVar RCV Id: RCV000674485
dbSNP Id: rs1582146275

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80106672_80106697del , CM000668.2:g.80106672_80106697del GRCh38
NC_000006.11:g.80816389_80816414del , CM000668.1:g.80816389_80816414del GRCh37
NC_000006.10:g.80873108_80873133del NCBI36
NG_009775.1:g.5046_5071del
NG_009775.2:g.5046_5071del

Transcript Alleles

HGVS Amino-acid change
ENST00000320393.9:c.-22_4del
ENST00000320393.8:c.-22_4del
ENST00000356489.9:c.-22_4del
ENST00000369760.8:c.-22_4del
NM_000056.3:c.-22_4del
NM_183050.2:c.-22_4del
XM_005248756.3:c.-22_4del
XM_006715542.2:c.-26_-15+14del
XM_011536023.1:c.-22_4del
XM_011536024.1:c.-22_4del
XM_011536025.1:c.-22_4del
XM_011536027.1:c.-22_4del
NM_000056.4:c.-22_4del
NM_001318975.1:c.-26_-15+14del
NM_183050.3:c.-22_4del
NR_134945.1:n.63_88del
XM_005248756.5:c.-22_4del
XM_011536023.3:c.-22_4del
XM_011536024.3:c.-22_4del
XM_011536025.3:c.-22_4del
XR_001743546.2:n.9_34del
XR_001743547.2:n.9_34del
XR_001743548.2:n.9_34del
XR_001743549.2:n.9_34del
XR_002956292.1:n.9_34del
NM_183050.4:c.-22_4del
NR_134945.2:n.2_27del
NM_000056.5:c.-22_4del