Canonical Allele Identifier: CA1641009922

Gene: BCKDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80343863T= , CM000668.2:g.80343863T=	GRCh38
NC_000006.11:g.81053580T= , CM000668.1:g.81053580T=	GRCh37
NC_000006.10:g.81110299T=	NCBI36
NG_009775.1:g.242237T=
NG_009775.2:g.242237T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.*59T= MANE Select	ENSP00000318351.5:n.*59T=
ENST00000320393.8:c.*59T=	ENSP00000318351.5:n.*59T=
ENST00000356489.9:c.*8+51T=	ENSP00000348880.5:n.*8+51T=
ENST00000491328.1:n.242+51T=
NM_000056.3:c.*8+51T=	NP_000047.1:n.*8+51T=
NM_183050.2:c.*59T=	NP_898871.1:n.*59T=
NM_000056.4:c.*8+51T=	NP_000047.1:n.*8+51T=
NM_001318975.1:c.*59T=	NP_001305904.1:n.*59T=
NM_183050.3:c.*59T=	NP_898871.1:n.*59T=
NR_134945.1:n.1416T=
XM_011536024.3:c.*244T=	XP_011534326.1:n.*244T=
XR_001743546.2:n.1068+70642T=
XR_001743547.2:n.1068+70642T=
XR_001743548.2:n.1068+70642T=
XR_001743549.2:n.1068+70642T=
XR_002956292.1:n.1068+70642T=
NM_183050.4:c.*59T= MANE Select	NP_898871.1:n.*59T=
NR_134945.2:n.1355T=
NM_000056.5:c.*8+51T=	NP_000047.1:n.*8+51T=