Canonical Allele Identifier: CA2336459259
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422748C= , CM000681.2:g.41422748C= GRCh38
NC_000019.9:g.41928653C= , CM000681.1:g.41928653C= GRCh37
NC_000019.8:g.46620493C= NCBI36
NG_013004.1:g.29960C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.973C= MANE Select ENSP00000269980.2:p.Leu325=
ENST00000269980.6:c.973C= ENSP00000269980.2:p.Leu325=
ENST00000457836.6:c.907C= ENSP00000416000.2:p.Leu303=
ENST00000535632.5:n.602C=
ENST00000540732.3:c.1075C= ENSP00000443246.1:p.Leu359=
ENST00000542943.5:c.886C= ENSP00000440345.1:p.Leu296=
ENST00000595085.5:c.922+51C= ENSP00000471150.2:n.922+51C=
NM_000709.3:c.973C= NP_000700.1:p.Leu325=
NM_001164783.1:c.970C= NP_001158255.1:p.Leu324=
NM_000709.4:c.973C= MANE Select NP_000700.1:p.Leu325=
NM_001164783.2:c.970C= NP_001158255.1:p.Leu324=