Canonical Allele Identifier: CA2336459080
Community Standard Title: NM_000709.4(BCKDHA):c.844G= (p.Asp282=)
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422361G= , CM000681.2:g.41422361G= GRCh38
NC_000019.9:g.41928266G= , CM000681.1:g.41928266G= GRCh37
NC_000019.8:g.46620106G= NCBI36
NG_013004.1:g.29573G=

Transcript Alleles

HGVS Amino-acid Change
NM_000709.4:c.844G= MANE Select NP_000700.1:p.Asp282=
ENST00000269980.7:c.844G= MANE Select ENSP00000269980.2:p.Asp282=
NM_000709.3:c.844G= NP_000700.1:p.Asp282=
NM_001164783.1:c.844G= NP_001158255.1:p.Asp282=
NM_001164783.2:c.844G= NP_001158255.1:p.Asp282=
ENST00000269980.6:c.844G= ENSP00000269980.2:p.Asp282=
ENST00000457836.6:c.778G= ENSP00000416000.2:p.Asp260=
ENST00000535632.5:n.473G=
ENST00000540732.3:c.946G= ENSP00000443246.1:p.Asp316=
ENST00000542943.5:c.757G= ENSP00000440345.1:p.Asp253=
ENST00000545787.1:n.472G=
ENST00000595085.5:c.844G= ENSP00000471150.2:p.Asp282=