Canonical Allele Identifier: CA224283

Gene: BCKDHB

Linked Data

• ClinVar Variation Id: 96584
• ClinVar RCV Id: RCV000179046
• dbSNP Id: rs398124577
• MyVariant Identifiers: chr6:g.80878602A>T (hg19) ; chr6:g.80168885A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80168885A>T , CM000668.2:g.80168885A>T	GRCh38
NC_000006.11:g.80878602A>T , CM000668.1:g.80878602A>T	GRCh37
NC_000006.10:g.80935321A>T	NCBI36
NG_009775.1:g.67259A>T
NG_009775.2:g.67259A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000320393.9:c.488A>T MANE Select	ENSP00000318351.5:p.Glu163Val
ENST00000320393.8:c.488A>T	ENSP00000318351.5:p.Glu163Val
ENST00000356489.9:c.488A>T	ENSP00000348880.5:p.Glu163Val
ENST00000369760.8:c.488A>T	ENSP00000358775.4:p.Glu163Val
NM_000056.3:c.488A>T	NP_000047.1:p.Glu163Val
NM_183050.2:c.488A>T	NP_898871.1:p.Glu163Val
XM_005248756.3:c.488A>T	XP_005248813.1:p.Glu163Val
XM_006715542.2:c.278A>T	XP_006715605.1:p.Glu93Val
XM_011536023.1:c.488A>T	XP_011534325.1:p.Glu163Val
XM_011536024.1:c.488A>T	XP_011534326.1:p.Glu163Val
XM_011536025.1:c.488A>T	XP_011534327.1:p.Glu163Val
XM_011536026.1:c.278A>T	XP_011534328.1:p.Glu93Val
XM_011536027.1:c.488A>T	XP_011534329.1:p.Glu163Val
NM_000056.4:c.488A>T	NP_000047.1:p.Glu163Val
NM_001318975.1:c.278A>T	NP_001305904.1:p.Glu93Val
NM_183050.3:c.488A>T	NP_898871.1:p.Glu163Val
NR_134945.1:n.572A>T
XM_005248756.5:c.488A>T	XP_005248813.1:p.Glu163Val
XM_011536023.3:c.488A>T	XP_011534325.1:p.Glu163Val
XM_011536024.3:c.488A>T	XP_011534326.1:p.Glu163Val
XM_011536025.3:c.488A>T	XP_011534327.1:p.Glu163Val
XR_001743546.2:n.518A>T
XR_001743547.2:n.518A>T
XR_001743548.2:n.518A>T
XR_001743549.2:n.518A>T
XR_002956292.1:n.518A>T
NM_183050.4:c.488A>T MANE Select	NP_898871.1:p.Glu163Val
NR_134945.2:n.511A>T
NM_000056.5:c.488A>T	NP_000047.1:p.Glu163Val