Canonical Allele Identifier: CA2336459013
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422230A= , CM000681.2:g.41422230A= GRCh38
NC_000019.9:g.41928135A= , CM000681.1:g.41928135A= GRCh37
NC_000019.8:g.46619975A= NCBI36
NG_013004.1:g.29442A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.713A= MANE Select ENSP00000269980.2:p.Glu238=
ENST00000269980.6:c.713A= ENSP00000269980.2:p.Glu238=
ENST00000457836.6:c.647A= ENSP00000416000.2:p.Glu216=
ENST00000535632.5:n.342A=
ENST00000540732.3:c.815A= ENSP00000443246.1:p.Glu272=
ENST00000541315.1:c.613A=
ENST00000542943.5:c.626A= ENSP00000440345.1:p.Glu209=
ENST00000545787.1:n.341A=
ENST00000595085.5:c.713A= ENSP00000471150.2:p.Glu238=
NM_000709.3:c.713A= NP_000700.1:p.Glu238=
NM_001164783.1:c.713A= NP_001158255.1:p.Glu238=
NM_000709.4:c.713A= MANE Select NP_000700.1:p.Glu238=
NM_001164783.2:c.713A= NP_001158255.1:p.Glu238=