Canonical Allele Identifier: CA1641009889

Gene: BCKDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80343830G= , CM000668.2:g.80343830G=	GRCh38
NC_000006.11:g.81053547G= , CM000668.1:g.81053547G=	GRCh37
NC_000006.10:g.81110266G=	NCBI36
NG_009775.1:g.242204G=
NG_009775.2:g.242204G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.*26G= MANE Select	ENSP00000318351.5:n.*26G=
ENST00000320393.8:c.*26G=	ENSP00000318351.5:n.*26G=
ENST00000356489.9:c.*8+18G=	ENSP00000348880.5:n.*8+18G=
ENST00000491328.1:n.242+18G=
NM_000056.3:c.*8+18G=	NP_000047.1:n.*8+18G=
NM_183050.2:c.*26G=	NP_898871.1:n.*26G=
NM_000056.4:c.*8+18G=	NP_000047.1:n.*8+18G=
NM_001318975.1:c.*26G=	NP_001305904.1:n.*26G=
NM_183050.3:c.*26G=	NP_898871.1:n.*26G=
NR_134945.1:n.1383G=
XM_011536024.3:c.*211G=	XP_011534326.1:n.*211G=
XR_001743546.2:n.1068+70609G=
XR_001743547.2:n.1068+70609G=
XR_001743548.2:n.1068+70609G=
XR_001743549.2:n.1068+70609G=
XR_002956292.1:n.1068+70609G=
NM_183050.4:c.*26G= MANE Select	NP_898871.1:n.*26G=
NR_134945.2:n.1322G=
NM_000056.5:c.*8+18G=	NP_000047.1:n.*8+18G=