Canonical Allele Identifier: CA2336458978
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422168G= , CM000681.2:g.41422168G= GRCh38
NC_000019.9:g.41928073G= , CM000681.1:g.41928073G= GRCh37
NC_000019.8:g.46619913G= NCBI36
NG_013004.1:g.29380G=

Transcript Alleles

HGVS Amino-acid change
ENST00000269980.7:c.651G= MANE Select ENSP00000269980.2:p.Val217=
ENST00000269980.6:c.651G= ENSP00000269980.2:p.Val217=
ENST00000457836.6:c.585G= ENSP00000416000.2:p.Val195=
ENST00000535632.5:n.280G=
ENST00000538423.5:n.777G=
ENST00000540732.3:c.753G= ENSP00000443246.1:p.Val251=
ENST00000541315.1:c.551G=
ENST00000542943.5:c.564G= ENSP00000440345.1:p.Val188=
ENST00000545787.1:n.279G=
ENST00000595085.5:c.651G= ENSP00000471150.2:p.Val217=
NM_000709.3:c.651G= NP_000700.1:p.Val217=
NM_001164783.1:c.651G= NP_001158255.1:p.Val217=
NM_000709.4:c.651G= MANE Select NP_000700.1:p.Val217=
NM_001164783.2:c.651G= NP_001158255.1:p.Val217=