Canonical Allele Identifier: CA2336459054
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422310C= , CM000681.2:g.41422310C= GRCh38
NC_000019.9:g.41928215C= , CM000681.1:g.41928215C= GRCh37
NC_000019.8:g.46620055C= NCBI36
NG_013004.1:g.29522C=

Transcript Alleles

HGVS Amino-acid change
ENST00000269980.7:c.793C= MANE Select ENSP00000269980.2:p.Arg265=
ENST00000269980.6:c.793C= ENSP00000269980.2:p.Arg265=
ENST00000457836.6:c.727C= ENSP00000416000.2:p.Arg243=
ENST00000535632.5:n.422C=
ENST00000540732.3:c.895C= ENSP00000443246.1:p.Arg299=
ENST00000542943.5:c.706C= ENSP00000440345.1:p.Arg236=
ENST00000545787.1:n.421C=
ENST00000595085.5:c.793C= ENSP00000471150.2:p.Arg265=
NM_000709.3:c.793C= NP_000700.1:p.Arg265=
NM_001164783.1:c.793C= NP_001158255.1:p.Arg265=
NM_000709.4:c.793C= MANE Select NP_000700.1:p.Arg265=
NM_001164783.2:c.793C= NP_001158255.1:p.Arg265=