Canonical Allele Identifier: CA1641009856

Gene: BCKDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80343800A= , CM000668.2:g.80343800A=	GRCh38
NC_000006.11:g.81053517A= , CM000668.1:g.81053517A=	GRCh37
NC_000006.10:g.81110236A=	NCBI36
NG_009775.1:g.242174A=
NG_009775.2:g.242174A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.1175A= MANE Select	ENSP00000318351.5:p.Tyr392=
ENST00000320393.8:c.1175A=	ENSP00000318351.5:p.Tyr392=
ENST00000356489.9:c.1175A=	ENSP00000348880.5:p.Tyr392=
ENST00000491328.1:n.230A=
NM_000056.3:c.1175A=	NP_000047.1:p.Tyr392=
NM_183050.2:c.1175A=	NP_898871.1:p.Tyr392=
XM_006715542.2:c.965A=	XP_006715605.1:p.Tyr322=
XM_011536024.1:c.*181A=	XP_011534326.1:n.*181A=
XM_011536026.1:c.965A=	XP_011534328.1:p.Tyr322=
NM_000056.4:c.1175A=	NP_000047.1:p.Tyr392=
NM_001318975.1:c.965A=	NP_001305904.1:p.Tyr322=
NM_183050.3:c.1175A=	NP_898871.1:p.Tyr392=
NR_134945.1:n.1353A=
XM_011536024.3:c.*181A=	XP_011534326.1:n.*181A=
XR_001743546.2:n.1068+70579A=
XR_001743547.2:n.1068+70579A=
XR_001743548.2:n.1068+70579A=
XR_001743549.2:n.1068+70579A=
XR_002956292.1:n.1068+70579A=
NM_183050.4:c.1175A= MANE Select	NP_898871.1:p.Tyr392=
NR_134945.2:n.1292A=
NM_000056.5:c.1175A=	NP_000047.1:p.Tyr392=