Canonical Allele Identifier: CA2695198301

Gene: BCKDHB

Linked Data

• ClinVar Variation Id: 2673069
• ClinVar RCV Id: RCV003457143

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80106856_80106859dup , CM000668.2:g.80106856_80106859dup	GRCh38
NC_000006.11:g.80816573_80816576dup , CM000668.1:g.80816573_80816576dup	GRCh37
NC_000006.10:g.80873292_80873295dup	NCBI36
NG_009775.1:g.5230_5233dup
NG_009775.2:g.5230_5233dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.163_166dup MANE Select	ENSP00000318351.5:p.Phe56TyrfsTer29
ENST00000320393.8:c.163_166dup	ENSP00000318351.5:p.Phe56TyrfsTer29
ENST00000356489.9:c.163_166dup	ENSP00000348880.5:p.Phe56TyrfsTer29
ENST00000369760.8:c.163_166dup	ENSP00000358775.4:p.Phe56TyrfsTer29
NM_000056.3:c.163_166dup	NP_000047.1:p.Phe56TyrfsTer29
NM_183050.2:c.163_166dup	NP_898871.1:p.Phe56TyrfsTer29
XM_005248756.3:c.163_166dup	XP_005248813.1:p.Phe56TyrfsTer29
XM_006715542.2:c.-15+173_-15+176dup	XP_006715605.1:n.-15+173_-15+176dup
XM_011536023.1:c.163_166dup	XP_011534325.1:p.Phe56TyrfsTer29
XM_011536024.1:c.163_166dup	XP_011534326.1:p.Phe56TyrfsTer29
XM_011536025.1:c.163_166dup	XP_011534327.1:p.Phe56TyrfsTer29
XM_011536027.1:c.163_166dup	XP_011534329.1:p.Phe56TyrfsTer29
NM_000056.4:c.163_166dup	NP_000047.1:p.Phe56TyrfsTer29
NM_001318975.1:c.-15+173_-15+176dup	NP_001305904.1:n.-15+173_-15+176dup
NM_183050.3:c.163_166dup	NP_898871.1:p.Phe56TyrfsTer29
NR_134945.1:n.247_250dup
XM_005248756.5:c.163_166dup	XP_005248813.1:p.Phe56TyrfsTer29
XM_011536023.3:c.163_166dup	XP_011534325.1:p.Phe56TyrfsTer29
XM_011536024.3:c.163_166dup	XP_011534326.1:p.Phe56TyrfsTer29
XM_011536025.3:c.163_166dup	XP_011534327.1:p.Phe56TyrfsTer29
XR_001743546.2:n.193_196dup
XR_001743547.2:n.193_196dup
XR_001743548.2:n.193_196dup
XR_001743549.2:n.193_196dup
XR_002956292.1:n.193_196dup
NM_183050.4:c.163_166dup MANE Select	NP_898871.1:p.Phe56TyrfsTer29
NR_134945.2:n.186_189dup
NM_000056.5:c.163_166dup	NP_000047.1:p.Phe56TyrfsTer29