Canonical Allele Identifier: CA2336460044
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424496T= , CM000681.2:g.41424496T= GRCh38
NC_000019.9:g.41930401T= , CM000681.1:g.41930401T= GRCh37
NC_000019.8:g.46622241T= NCBI36
NG_013004.1:g.31708T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1226T= MANE Select ENSP00000269980.2:p.Phe409=
ENST00000269980.6:c.1226T= ENSP00000269980.2:p.Phe409=
ENST00000457836.6:c.1235T= ENSP00000416000.2:p.Phe412=
ENST00000540732.3:c.1328T= ENSP00000443246.1:p.Phe443=
ENST00000544905.1:c.62-6T=
ENST00000595085.5:c.922+1799T= ENSP00000471150.2:n.922+1799T=
NM_000709.3:c.1226T= NP_000700.1:p.Phe409=
NM_001164783.1:c.1223T= NP_001158255.1:p.Phe408=
NM_000709.4:c.1226T= MANE Select NP_000700.1:p.Phe409=
NM_001164783.2:c.1223T= NP_001158255.1:p.Phe408=