Canonical Allele Identifier: CA1640938904

Gene: BCKDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80171369A= , CM000668.2:g.80171369A=	GRCh38
NC_000006.11:g.80881086A= , CM000668.1:g.80881086A=	GRCh37
NC_000006.10:g.80937805A=	NCBI36
NG_009775.1:g.69743A=
NG_009775.2:g.69743A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.721A= MANE Select	ENSP00000318351.5:p.Lys241=
ENST00000320393.8:c.721A=	ENSP00000318351.5:p.Lys241=
ENST00000356489.9:c.721A=	ENSP00000348880.5:p.Lys241=
NM_000056.3:c.721A=	NP_000047.1:p.Lys241=
NM_183050.2:c.721A=	NP_898871.1:p.Lys241=
XM_005248756.3:c.721A=	XP_005248813.1:p.Lys241=
XM_006715542.2:c.511A=	XP_006715605.1:p.Lys171=
XM_011536023.1:c.721A=	XP_011534325.1:p.Lys241=
XM_011536024.1:c.721A=	XP_011534326.1:p.Lys241=
XM_011536025.1:c.721A=	XP_011534327.1:p.Lys241=
XM_011536026.1:c.511A=	XP_011534328.1:p.Lys171=
NM_000056.4:c.721A=	NP_000047.1:p.Lys241=
NM_001318975.1:c.511A=	NP_001305904.1:p.Lys171=
NM_183050.3:c.721A=	NP_898871.1:p.Lys241=
NR_134945.1:n.899A=
XM_005248756.5:c.721A=	XP_005248813.1:p.Lys241=
XM_011536023.3:c.721A=	XP_011534325.1:p.Lys241=
XM_011536024.3:c.721A=	XP_011534326.1:p.Lys241=
XM_011536025.3:c.721A=	XP_011534327.1:p.Lys241=
XR_001743546.2:n.751A=
XR_001743547.2:n.751A=
XR_001743548.2:n.751A=
XR_001743549.2:n.751A=
XR_002956292.1:n.751A=
NM_183050.4:c.721A= MANE Select	NP_898871.1:p.Lys241=
NR_134945.2:n.838A=
NM_000056.5:c.721A=	NP_000047.1:p.Lys241=