Canonical Allele Identifier: CA2336453738
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41410612T= , CM000681.2:g.41410612T= GRCh38
NC_000019.9:g.41916517T= , CM000681.1:g.41916517T= GRCh37
NC_000019.8:g.46608357T= NCBI36
NG_013004.1:g.17824T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.109-25T= MANE Select ENSP00000269980.2:n.109-25T=
ENST00000269980.6:c.109-25T= ENSP00000269980.2:n.109-25T=
ENST00000457836.6:c.58-40T= ENSP00000416000.2:n.58-40T=
ENST00000538423.5:n.129-25T=
ENST00000540732.3:c.211-25T= ENSP00000443246.1:n.211-25T=
ENST00000542943.5:c.109-25T= ENSP00000440345.1:n.109-25T=
ENST00000595085.5:c.109-25T= ENSP00000471150.2:n.109-25T=
ENST00000604424.1:n.351-25T=
NM_000709.3:c.109-25T= NP_000700.1:n.109-25T=
NM_001164783.1:c.109-25T= NP_001158255.1:n.109-25T=
NM_000709.4:c.109-25T= MANE Select NP_000700.1:n.109-25T=
NM_001164783.2:c.109-25T= NP_001158255.1:n.109-25T=