Canonical Allele Identifier: CA2336459045
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422285T= , CM000681.2:g.41422285T= GRCh38
NC_000019.9:g.41928190T= , CM000681.1:g.41928190T= GRCh37
NC_000019.8:g.46620030T= NCBI36
NG_013004.1:g.29497T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.768T= MANE Select ENSP00000269980.2:p.Leu256=
ENST00000269980.6:c.768T= ENSP00000269980.2:p.Leu256=
ENST00000457836.6:c.702T= ENSP00000416000.2:p.Leu234=
ENST00000535632.5:n.397T=
ENST00000540732.3:c.870T= ENSP00000443246.1:p.Leu290=
ENST00000542943.5:c.681T= ENSP00000440345.1:p.Leu227=
ENST00000545787.1:n.396T=
ENST00000595085.5:c.768T= ENSP00000471150.2:p.Leu256=
NM_000709.3:c.768T= NP_000700.1:p.Leu256=
NM_001164783.1:c.768T= NP_001158255.1:p.Leu256=
NM_000709.4:c.768T= MANE Select NP_000700.1:p.Leu256=
NM_001164783.2:c.768T= NP_001158255.1:p.Leu256=