Canonical Allele Identifier: CA2581387369
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422796C>G , CM000681.2:g.41422796C>G GRCh38
NC_000019.9:g.41928701C>G , CM000681.1:g.41928701C>G GRCh37
NC_000019.8:g.46620541C>G NCBI36
NG_013004.1:g.30008C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.995+26C>G MANE Select ENSP00000269980.2:n.995+26C>G
ENST00000269980.6:c.995+26C>G ENSP00000269980.2:n.995+26C>G
ENST00000457836.6:c.929+26C>G ENSP00000416000.2:n.929+26C>G
ENST00000540732.3:c.1097+26C>G ENSP00000443246.1:n.1097+26C>G
ENST00000542943.5:c.908+26C>G ENSP00000440345.1:n.908+26C>G
ENST00000595085.5:c.922+99C>G ENSP00000471150.2:n.922+99C>G
NM_000709.3:c.995+26C>G NP_000700.1:n.995+26C>G
NM_001164783.1:c.992+26C>G NP_001158255.1:n.992+26C>G
NM_000709.4:c.995+26C>G MANE Select NP_000700.1:n.995+26C>G
NM_001164783.2:c.992+26C>G NP_001158255.1:n.992+26C>G