Canonical Allele Identifier: CA2336459206
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422644G= , CM000681.2:g.41422644G= GRCh38
NC_000019.9:g.41928549G= , CM000681.1:g.41928549G= GRCh37
NC_000019.8:g.46620389G= NCBI36
NG_013004.1:g.29856G=

Transcript Alleles

HGVS Amino-acid change
ENST00000269980.7:c.869G= MANE Select ENSP00000269980.2:p.Gly290=
ENST00000269980.6:c.869G= ENSP00000269980.2:p.Gly290=
ENST00000457836.6:c.803G= ENSP00000416000.2:p.Gly268=
ENST00000535632.5:n.498G=
ENST00000540732.3:c.971G= ENSP00000443246.1:p.Gly324=
ENST00000542943.5:c.782G= ENSP00000440345.1:p.Gly261=
ENST00000545787.1:n.497G=
ENST00000595085.5:c.869G= ENSP00000471150.2:p.Gly290=
NM_000709.3:c.869G= NP_000700.1:p.Gly290=
NM_001164783.1:c.866G= NP_001158255.1:p.Gly289=
NM_000709.4:c.869G= MANE Select NP_000700.1:p.Gly290=
NM_001164783.2:c.866G= NP_001158255.1:p.Gly289=