Canonical Allele Identifier: CA2336458989
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422187A= , CM000681.2:g.41422187A= GRCh38
NC_000019.9:g.41928092A= , CM000681.1:g.41928092A= GRCh37
NC_000019.8:g.46619932A= NCBI36
NG_013004.1:g.29399A=

Transcript Alleles

HGVS Amino-acid change
ENST00000269980.7:c.670A= MANE Select ENSP00000269980.2:p.Lys224=
ENST00000269980.6:c.670A= ENSP00000269980.2:p.Lys224=
ENST00000457836.6:c.604A= ENSP00000416000.2:p.Lys202=
ENST00000535632.5:n.299A=
ENST00000538423.5:n.796A=
ENST00000540732.3:c.772A= ENSP00000443246.1:p.Lys258=
ENST00000541315.1:c.570A=
ENST00000542943.5:c.583A= ENSP00000440345.1:p.Lys195=
ENST00000545787.1:n.298A=
ENST00000595085.5:c.670A= ENSP00000471150.2:p.Lys224=
NM_000709.3:c.670A= NP_000700.1:p.Lys224=
NM_001164783.1:c.670A= NP_001158255.1:p.Lys224=
NM_000709.4:c.670A= MANE Select NP_000700.1:p.Lys224=
NM_001164783.2:c.670A= NP_001158255.1:p.Lys224=