Canonical Allele Identifier: CA2336453942
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41410984G= , CM000681.2:g.41410984G= GRCh38
NC_000019.9:g.41916889G= , CM000681.1:g.41916889G= GRCh37
NC_000019.8:g.46608729G= NCBI36
NG_013004.1:g.18196G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.350G= MANE Select ENSP00000269980.2:p.Arg117=
ENST00000269980.6:c.350G= ENSP00000269980.2:p.Arg117=
ENST00000457836.6:c.284G= ENSP00000416000.2:p.Arg95=
ENST00000538423.5:n.476G=
ENST00000540732.3:c.452G= ENSP00000443246.1:p.Arg151=
ENST00000541315.1:c.157G=
ENST00000542943.5:c.288+168G= ENSP00000440345.1:n.288+168G=
ENST00000595085.5:c.350G= ENSP00000471150.2:p.Arg117=
NM_000709.3:c.350G= NP_000700.1:p.Arg117=
NM_001164783.1:c.350G= NP_001158255.1:p.Arg117=
NM_000709.4:c.350G= MANE Select NP_000700.1:p.Arg117=
NM_001164783.2:c.350G= NP_001158255.1:p.Arg117=