Canonical Allele Identifier: CA2336459231
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422696C= , CM000681.2:g.41422696C= GRCh38
NC_000019.9:g.41928601C= , CM000681.1:g.41928601C= GRCh37
NC_000019.8:g.46620441C= NCBI36
NG_013004.1:g.29908C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.921C= MANE Select ENSP00000269980.2:p.Tyr307=
ENST00000269980.6:c.921C= ENSP00000269980.2:p.Tyr307=
ENST00000457836.6:c.855C= ENSP00000416000.2:p.Tyr285=
ENST00000535632.5:n.550C=
ENST00000540732.3:c.1023C= ENSP00000443246.1:p.Tyr341=
ENST00000542943.5:c.834C= ENSP00000440345.1:p.Tyr278=
ENST00000545787.1:n.549C=
ENST00000595085.5:c.921C= ENSP00000471150.2:p.Tyr307=
NM_000709.3:c.921C= NP_000700.1:p.Tyr307=
NM_001164783.1:c.918C= NP_001158255.1:p.Tyr306=
NM_000709.4:c.921C= MANE Select NP_000700.1:p.Tyr307=
NM_001164783.2:c.918C= NP_001158255.1:p.Tyr306=