Canonical Allele Identifier: CA2336458994
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422191G= , CM000681.2:g.41422191G= GRCh38
NC_000019.9:g.41928096G= , CM000681.1:g.41928096G= GRCh37
NC_000019.8:g.46619936G= NCBI36
NG_013004.1:g.29403G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.674G= MANE Select ENSP00000269980.2:p.Arg225=
ENST00000269980.6:c.674G= ENSP00000269980.2:p.Arg225=
ENST00000457836.6:c.608G= ENSP00000416000.2:p.Arg203=
ENST00000535632.5:n.303G=
ENST00000538423.5:n.800G=
ENST00000540732.3:c.776G= ENSP00000443246.1:p.Arg259=
ENST00000541315.1:c.574G=
ENST00000542943.5:c.587G= ENSP00000440345.1:p.Arg196=
ENST00000545787.1:n.302G=
ENST00000595085.5:c.674G= ENSP00000471150.2:p.Arg225=
NM_000709.3:c.674G= NP_000700.1:p.Arg225=
NM_001164783.1:c.674G= NP_001158255.1:p.Arg225=
NM_000709.4:c.674G= MANE Select NP_000700.1:p.Arg225=
NM_001164783.2:c.674G= NP_001158255.1:p.Arg225=