Canonical Allele Identifier: CA2573141188

Gene: BCKDHB

Linked Data

• ClinVar Variation Id: 1413124
• ClinVar RCV Id: RCV001943366
• dbSNP Id: rs2127775550

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80168922dup , CM000668.2:g.80168922dup	GRCh38
NC_000006.11:g.80878639dup , CM000668.1:g.80878639dup	GRCh37
NC_000006.10:g.80935358dup	NCBI36
NG_009775.1:g.67296dup
NG_009775.2:g.67296dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.525dup MANE Select	ENSP00000318351.5:p.Asn176Ter
ENST00000320393.8:c.525dup	ENSP00000318351.5:p.Asn176Ter
ENST00000356489.9:c.525dup	ENSP00000348880.5:p.Asn176Ter
ENST00000369760.8:c.525dup	ENSP00000358775.4:p.Asn176Ter
NM_000056.3:c.525dup	NP_000047.1:p.Asn176Ter
NM_183050.2:c.525dup	NP_898871.1:p.Asn176Ter
XM_005248756.3:c.525dup	XP_005248813.1:p.Asn176Ter
XM_006715542.2:c.315dup	XP_006715605.1:p.Asn106Ter
XM_011536023.1:c.525dup	XP_011534325.1:p.Asn176Ter
XM_011536024.1:c.525dup	XP_011534326.1:p.Asn176Ter
XM_011536025.1:c.525dup	XP_011534327.1:p.Asn176Ter
XM_011536026.1:c.315dup	XP_011534328.1:p.Asn106Ter
XM_011536027.1:c.525dup	XP_011534329.1:p.Asn176Ter
NM_000056.4:c.525dup	NP_000047.1:p.Asn176Ter
NM_001318975.1:c.315dup	NP_001305904.1:p.Asn106Ter
NM_183050.3:c.525dup	NP_898871.1:p.Asn176Ter
NR_134945.1:n.609dup
XM_005248756.5:c.525dup	XP_005248813.1:p.Asn176Ter
XM_011536023.3:c.525dup	XP_011534325.1:p.Asn176Ter
XM_011536024.3:c.525dup	XP_011534326.1:p.Asn176Ter
XM_011536025.3:c.525dup	XP_011534327.1:p.Asn176Ter
XR_001743546.2:n.555dup
XR_001743547.2:n.555dup
XR_001743548.2:n.555dup
XR_001743549.2:n.555dup
XR_002956292.1:n.555dup
NM_183050.4:c.525dup MANE Select	NP_898871.1:p.Asn176Ter
NR_134945.2:n.548dup
NM_000056.5:c.525dup	NP_000047.1:p.Asn176Ter