Canonical Allele Identifier: CA2336458985
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422178T= , CM000681.2:g.41422178T= GRCh38
NC_000019.9:g.41928083T= , CM000681.1:g.41928083T= GRCh37
NC_000019.8:g.46619923T= NCBI36
NG_013004.1:g.29390T=

Transcript Alleles

HGVS Amino-acid change
ENST00000269980.7:c.661T= MANE Select ENSP00000269980.2:p.Tyr221=
ENST00000269980.6:c.661T= ENSP00000269980.2:p.Tyr221=
ENST00000457836.6:c.595T= ENSP00000416000.2:p.Tyr199=
ENST00000535632.5:n.290T=
ENST00000538423.5:n.787T=
ENST00000540732.3:c.763T= ENSP00000443246.1:p.Tyr255=
ENST00000541315.1:c.561T=
ENST00000542943.5:c.574T= ENSP00000440345.1:p.Tyr192=
ENST00000545787.1:n.289T=
ENST00000595085.5:c.661T= ENSP00000471150.2:p.Tyr221=
NM_000709.3:c.661T= NP_000700.1:p.Tyr221=
NM_001164783.1:c.661T= NP_001158255.1:p.Tyr221=
NM_000709.4:c.661T= MANE Select NP_000700.1:p.Tyr221=
NM_001164783.2:c.661T= NP_001158255.1:p.Tyr221=