Canonical Allele Identifier: CA2336459051
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422301T= , CM000681.2:g.41422301T= GRCh38
NC_000019.9:g.41928206T= , CM000681.1:g.41928206T= GRCh37
NC_000019.8:g.46620046T= NCBI36
NG_013004.1:g.29513T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.784T= MANE Select ENSP00000269980.2:p.Phe262=
ENST00000269980.6:c.784T= ENSP00000269980.2:p.Phe262=
ENST00000457836.6:c.718T= ENSP00000416000.2:p.Phe240=
ENST00000535632.5:n.413T=
ENST00000540732.3:c.886T= ENSP00000443246.1:p.Phe296=
ENST00000542943.5:c.697T= ENSP00000440345.1:p.Phe233=
ENST00000545787.1:n.412T=
ENST00000595085.5:c.784T= ENSP00000471150.2:p.Phe262=
NM_000709.3:c.784T= NP_000700.1:p.Phe262=
NM_001164783.1:c.784T= NP_001158255.1:p.Phe262=
NM_000709.4:c.784T= MANE Select NP_000700.1:p.Phe262=
NM_001164783.2:c.784T= NP_001158255.1:p.Phe262=