Canonical Allele Identifier: CA1640953009

Gene: BCKDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80203114C= , CM000668.2:g.80203114C=	GRCh38
NC_000006.11:g.80912831C= , CM000668.1:g.80912831C=	GRCh37
NC_000006.10:g.80969550C=	NCBI36
NG_009775.1:g.101488C=
NG_009775.2:g.101488C=

Transcript Alleles

HGVS	Amino-acid Change
NM_183050.4:c.853C= MANE Select	NP_898871.1:p.Arg285=
ENST00000320393.9:c.853C= MANE Select	ENSP00000318351.5:p.Arg285=
NM_000056.3:c.853C=	NP_000047.1:p.Arg285=
NM_000056.4:c.853C=	NP_000047.1:p.Arg285=
NM_000056.5:c.853C=	NP_000047.1:p.Arg285=
NM_001318975.1:c.643C=	NP_001305904.1:p.Arg215=
NM_183050.2:c.853C=	NP_898871.1:p.Arg285=
NM_183050.3:c.853C=	NP_898871.1:p.Arg285=
NR_134945.1:n.1031C=
NR_134945.2:n.970C=
ENST00000320393.8:c.853C=	ENSP00000318351.5:p.Arg285=
ENST00000356489.9:c.853C=	ENSP00000348880.5:p.Arg285=
ENST00000468520.1:n.13C=
XM_005248756.3:c.853C=	XP_005248813.1:p.Arg285=
XM_005248756.5:c.853C=	XP_005248813.1:p.Arg285=
XM_006715542.2:c.643C=	XP_006715605.1:p.Arg215=
XM_011536023.1:c.853C=	XP_011534325.1:p.Arg285=
XM_011536023.3:c.853C=	XP_011534325.1:p.Arg285=
XM_011536024.1:c.853C=	XP_011534326.1:p.Arg285=
XM_011536024.3:c.853C=	XP_011534326.1:p.Arg285=
XM_011536025.1:c.853C=	XP_011534327.1:p.Arg285=
XM_011536025.3:c.853C=	XP_011534327.1:p.Arg285=
XM_011536026.1:c.643C=	XP_011534328.1:p.Arg215=
XR_001743546.2:n.883C=
XR_001743547.2:n.883C=
XR_001743548.2:n.883C=
XR_001743549.2:n.883C=
XR_002956292.1:n.883C=