Canonical Allele Identifier: CA2336459299

Gene: BCKDHA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422814C= , CM000681.2:g.41422814C=	GRCh38
NC_000019.9:g.41928719C= , CM000681.1:g.41928719C=	GRCh37
NC_000019.8:g.46620559C=	NCBI36
NG_013004.1:g.30026C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.995+44C= MANE Select	ENSP00000269980.2:n.995+44C=
ENST00000269980.6:c.995+44C=	ENSP00000269980.2:n.995+44C=
ENST00000457836.6:c.929+44C=	ENSP00000416000.2:n.929+44C=
ENST00000540732.3:c.1097+44C=	ENSP00000443246.1:n.1097+44C=
ENST00000542943.5:c.908+44C=	ENSP00000440345.1:n.908+44C=
ENST00000595085.5:c.922+117C=	ENSP00000471150.2:n.922+117C=
NM_000709.3:c.995+44C=	NP_000700.1:n.995+44C=
NM_001164783.1:c.992+44C=	NP_001158255.1:n.992+44C=
NM_000709.4:c.995+44C= MANE Select	NP_000700.1:n.995+44C=
NM_001164783.2:c.992+44C=	NP_001158255.1:n.992+44C=