Canonical Allele Identifier: CA1640984706

Gene: BCKDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80273124T= , CM000668.2:g.80273124T=	GRCh38
NC_000006.11:g.80982841T= , CM000668.1:g.80982841T=	GRCh37
NC_000006.10:g.81039560T=	NCBI36
NG_009775.1:g.171498T=
NG_009775.2:g.171498T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.952-11T= MANE Select	ENSP00000318351.5:n.952-11T=
ENST00000320393.8:c.952-11T=	ENSP00000318351.5:n.952-11T=
ENST00000356489.9:c.952-11T=	ENSP00000348880.5:n.952-11T=
ENST00000468520.1:n.182-11T=
NM_000056.3:c.952-11T=	NP_000047.1:n.952-11T=
NM_183050.2:c.952-11T=	NP_898871.1:n.952-11T=
XM_005248756.3:c.952-11T=	XP_005248813.1:n.952-11T=
XM_006715542.2:c.742-11T=	XP_006715605.1:n.742-11T=
XM_011536023.1:c.952-11T=	XP_011534325.1:n.952-11T=
XM_011536024.1:c.952-11T=	XP_011534326.1:n.952-11T=
XM_011536025.1:c.952-11T=	XP_011534327.1:n.952-11T=
XM_011536026.1:c.742-11T=	XP_011534328.1:n.742-11T=
NM_000056.4:c.952-11T=	NP_000047.1:n.952-11T=
NM_001318975.1:c.742-11T=	NP_001305904.1:n.742-11T=
NM_183050.3:c.952-11T=	NP_898871.1:n.952-11T=
NR_134945.1:n.1130-11T=
XM_005248756.5:c.952-11T=	XP_005248813.1:n.952-11T=
XM_011536023.3:c.952-11T=	XP_011534325.1:n.952-11T=
XM_011536024.3:c.952-11T=	XP_011534326.1:n.952-11T=
XM_011536025.3:c.952-11T=	XP_011534327.1:n.952-11T=
XR_001743546.2:n.982-11T=
XR_001743547.2:n.982-11T=
XR_001743548.2:n.982-11T=
XR_001743549.2:n.982-11T=
XR_002956292.1:n.982-11T=
NM_183050.4:c.952-11T= MANE Select	NP_898871.1:n.952-11T=
NR_134945.2:n.1069-11T=
NM_000056.5:c.952-11T=	NP_000047.1:n.952-11T=