Canonical Allele Identifier: CA2336459202
Community Standard Title: NM_000709.4(BCKDHA):c.859C= (p.Arg287=)
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422634C= , CM000681.2:g.41422634C= GRCh38
NC_000019.9:g.41928539C= , CM000681.1:g.41928539C= GRCh37
NC_000019.8:g.46620379C= NCBI36
NG_013004.1:g.29846C=

Transcript Alleles

HGVS Amino-acid Change
NM_000709.4:c.859C= MANE Select NP_000700.1:p.Arg287=
ENST00000269980.7:c.859C= MANE Select ENSP00000269980.2:p.Arg287=
NM_000709.3:c.859C= NP_000700.1:p.Arg287=
NM_001164783.1:c.856C= NP_001158255.1:p.Arg286=
NM_001164783.2:c.856C= NP_001158255.1:p.Arg286=
ENST00000269980.6:c.859C= ENSP00000269980.2:p.Arg287=
ENST00000457836.6:c.793C= ENSP00000416000.2:p.Arg265=
ENST00000535632.5:n.488C=
ENST00000540732.3:c.961C= ENSP00000443246.1:p.Arg321=
ENST00000542943.5:c.772C= ENSP00000440345.1:p.Arg258=
ENST00000545787.1:n.487C=
ENST00000595085.5:c.859C= ENSP00000471150.2:p.Arg287=