Canonical Allele Identifier: CA658821864
Gene: BCKDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 556787
ClinVar RCV Id: RCV000672840
dbSNP Id: rs1554189447
MyVariant Identifiers: chr6:g.80167698dup (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80167698dup , CM000668.2:g.80167698dup GRCh38
NC_000006.11:g.80877415dup , CM000668.1:g.80877415dup GRCh37
NC_000006.10:g.80934134dup NCBI36
NG_009775.1:g.66072dup
NG_009775.2:g.66072dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000320393.9:c.364dup MANE Select ENSP00000318351.5:p.Thr122AsnfsTer5
ENST00000320393.8:c.364dup ENSP00000318351.5:p.Thr122AsnfsTer5
ENST00000356489.9:c.364dup ENSP00000348880.5:p.Thr122AsnfsTer5
ENST00000369760.8:c.364dup ENSP00000358775.4:p.Thr122AsnfsTer5
NM_000056.3:c.364dup NP_000047.1:p.Thr122AsnfsTer5
NM_183050.2:c.364dup NP_898871.1:p.Thr122AsnfsTer5
XM_005248756.3:c.364dup XP_005248813.1:p.Thr122AsnfsTer5
XM_006715542.2:c.154dup XP_006715605.1:p.Thr52AsnfsTer5
XM_011536023.1:c.364dup XP_011534325.1:p.Thr122AsnfsTer5
XM_011536024.1:c.364dup XP_011534326.1:p.Thr122AsnfsTer5
XM_011536025.1:c.364dup XP_011534327.1:p.Thr122AsnfsTer5
XM_011536026.1:c.154dup XP_011534328.1:p.Thr52AsnfsTer5
XM_011536027.1:c.364dup XP_011534329.1:p.Thr122AsnfsTer5
NM_000056.4:c.364dup NP_000047.1:p.Thr122AsnfsTer5
NM_001318975.1:c.154dup NP_001305904.1:p.Thr52AsnfsTer5
NM_183050.3:c.364dup NP_898871.1:p.Thr122AsnfsTer5
NR_134945.1:n.448dup
XM_005248756.5:c.364dup XP_005248813.1:p.Thr122AsnfsTer5
XM_011536023.3:c.364dup XP_011534325.1:p.Thr122AsnfsTer5
XM_011536024.3:c.364dup XP_011534326.1:p.Thr122AsnfsTer5
XM_011536025.3:c.364dup XP_011534327.1:p.Thr122AsnfsTer5
XR_001743546.2:n.394dup
XR_001743547.2:n.394dup
XR_001743548.2:n.394dup
XR_001743549.2:n.394dup
XR_002956292.1:n.394dup
NM_183050.4:c.364dup MANE Select NP_898871.1:p.Thr122AsnfsTer5
NR_134945.2:n.387dup
NM_000056.5:c.364dup NP_000047.1:p.Thr122AsnfsTer5