Canonical Allele Identifier: CA224309

Gene: BCKDHB

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80168923A>T , CM000668.2:g.80168923A>T	GRCh38
NC_000006.11:g.80878640A>T , CM000668.1:g.80878640A>T	GRCh37
NC_000006.10:g.80935359A>T	NCBI36
NG_009775.1:g.67297A>T
NG_009775.2:g.67297A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.526A>T MANE Select	ENSP00000318351.5:p.Asn176Tyr
ENST00000320393.8:c.526A>T	ENSP00000318351.5:p.Asn176Tyr
ENST00000356489.9:c.526A>T	ENSP00000348880.5:p.Asn176Tyr
ENST00000369760.8:c.526A>T	ENSP00000358775.4:p.Asn176Tyr
NM_000056.3:c.526A>T	NP_000047.1:p.Asn176Tyr
NM_183050.2:c.526A>T	NP_898871.1:p.Asn176Tyr
XM_005248756.3:c.526A>T	XP_005248813.1:p.Asn176Tyr
XM_006715542.2:c.316A>T	XP_006715605.1:p.Asn106Tyr
XM_011536023.1:c.526A>T	XP_011534325.1:p.Asn176Tyr
XM_011536024.1:c.526A>T	XP_011534326.1:p.Asn176Tyr
XM_011536025.1:c.526A>T	XP_011534327.1:p.Asn176Tyr
XM_011536026.1:c.316A>T	XP_011534328.1:p.Asn106Tyr
XM_011536027.1:c.526A>T	XP_011534329.1:p.Asn176Tyr
NM_000056.4:c.526A>T	NP_000047.1:p.Asn176Tyr
NM_001318975.1:c.316A>T	NP_001305904.1:p.Asn106Tyr
NM_183050.3:c.526A>T	NP_898871.1:p.Asn176Tyr
NR_134945.1:n.610A>T
XM_005248756.5:c.526A>T	XP_005248813.1:p.Asn176Tyr
XM_011536023.3:c.526A>T	XP_011534325.1:p.Asn176Tyr
XM_011536024.3:c.526A>T	XP_011534326.1:p.Asn176Tyr
XM_011536025.3:c.526A>T	XP_011534327.1:p.Asn176Tyr
XR_001743546.2:n.556A>T
XR_001743547.2:n.556A>T
XR_001743548.2:n.556A>T
XR_001743549.2:n.556A>T
XR_002956292.1:n.556A>T
NM_183050.4:c.526A>T MANE Select	NP_898871.1:p.Asn176Tyr
NR_134945.2:n.549A>T
NM_000056.5:c.526A>T	NP_000047.1:p.Asn176Tyr