Canonical Allele Identifier: CA2336459075
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422356G= , CM000681.2:g.41422356G= GRCh38
NC_000019.9:g.41928261G= , CM000681.1:g.41928261G= GRCh37
NC_000019.8:g.46620101G= NCBI36
NG_013004.1:g.29568G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.839G= MANE Select ENSP00000269980.2:p.Arg280=
ENST00000269980.6:c.839G= ENSP00000269980.2:p.Arg280=
ENST00000457836.6:c.773G= ENSP00000416000.2:p.Arg258=
ENST00000535632.5:n.468G=
ENST00000540732.3:c.941G= ENSP00000443246.1:p.Arg314=
ENST00000542943.5:c.752G= ENSP00000440345.1:p.Arg251=
ENST00000545787.1:n.467G=
ENST00000595085.5:c.839G= ENSP00000471150.2:p.Arg280=
NM_000709.3:c.839G= NP_000700.1:p.Arg280=
NM_001164783.1:c.839G= NP_001158255.1:p.Arg280=
NM_000709.4:c.839G= MANE Select NP_000700.1:p.Arg280=
NM_001164783.2:c.839G= NP_001158255.1:p.Arg280=