Canonical Allele Identifier: CA2336460031
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424466G= , CM000681.2:g.41424466G= GRCh38
NC_000019.9:g.41930371G= , CM000681.1:g.41930371G= GRCh37
NC_000019.8:g.46622211G= NCBI36
NG_013004.1:g.31678G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1196G= MANE Select ENSP00000269980.2:p.Arg399=
ENST00000269980.6:c.1196G= ENSP00000269980.2:p.Arg399=
ENST00000457836.6:c.1205G= ENSP00000416000.2:p.Arg402=
ENST00000540732.3:c.1298G= ENSP00000443246.1:p.Arg433=
ENST00000544905.1:c.62-36G=
ENST00000595085.5:c.922+1769G= ENSP00000471150.2:n.922+1769G=
NM_000709.3:c.1196G= NP_000700.1:p.Arg399=
NM_001164783.1:c.1193G= NP_001158255.1:p.Arg398=
NM_000709.4:c.1196G= MANE Select NP_000700.1:p.Arg399=
NM_001164783.2:c.1193G= NP_001158255.1:p.Arg398=