Canonical Allele Identifier: CA2336453796
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41410726A= , CM000681.2:g.41410726A= GRCh38
NC_000019.9:g.41916631A= , CM000681.1:g.41916631A= GRCh37
NC_000019.8:g.46608471A= NCBI36
NG_013004.1:g.17938A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.198A= MANE Select ENSP00000269980.2:p.Glu66=
ENST00000269980.6:c.198A= ENSP00000269980.2:p.Glu66=
ENST00000457836.6:c.132A= ENSP00000416000.2:p.Glu44=
ENST00000538423.5:n.218A=
ENST00000540732.3:c.300A= ENSP00000443246.1:p.Glu100=
ENST00000541315.1:c.5A=
ENST00000542943.5:c.198A= ENSP00000440345.1:p.Glu66=
ENST00000595085.5:c.198A= ENSP00000471150.2:p.Glu66=
ENST00000604424.1:n.440A=
NM_000709.3:c.198A= NP_000700.1:p.Glu66=
NM_001164783.1:c.198A= NP_001158255.1:p.Glu66=
NM_000709.4:c.198A= MANE Select NP_000700.1:p.Glu66=
NM_001164783.2:c.198A= NP_001158255.1:p.Glu66=