Canonical Allele Identifier: CA2336460094
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424599C= , CM000681.2:g.41424599C= GRCh38
NC_000019.9:g.41930504C= , CM000681.1:g.41930504C= GRCh37
NC_000019.8:g.46622344C= NCBI36
NG_013004.1:g.31811C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1329C= MANE Select ENSP00000269980.2:p.Phe443=
ENST00000269980.6:c.1329C= ENSP00000269980.2:p.Phe443=
ENST00000457836.6:c.1338C= ENSP00000416000.2:p.Phe446=
ENST00000540732.3:c.1431C= ENSP00000443246.1:p.Phe477=
ENST00000544905.1:c.159C=
ENST00000595085.5:c.922+1902C= ENSP00000471150.2:n.922+1902C=
NM_000709.3:c.1329C= NP_000700.1:p.Phe443=
NM_001164783.1:c.1326C= NP_001158255.1:p.Phe442=
NM_000709.4:c.1329C= MANE Select NP_000700.1:p.Phe443=
NM_001164783.2:c.1326C= NP_001158255.1:p.Phe442=