Canonical Allele Identifier: CA2336453849
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41410828C= , CM000681.2:g.41410828C= GRCh38
NC_000019.9:g.41916733C= , CM000681.1:g.41916733C= GRCh37
NC_000019.8:g.46608573C= NCBI36
NG_013004.1:g.18040C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.288+12C= MANE Select ENSP00000269980.2:n.288+12C=
ENST00000269980.6:c.288+12C= ENSP00000269980.2:n.288+12C=
ENST00000457836.6:c.222+12C= ENSP00000416000.2:n.222+12C=
ENST00000538423.5:n.320C=
ENST00000540732.3:c.390+12C= ENSP00000443246.1:n.390+12C=
ENST00000541315.1:c.95+12C=
ENST00000542943.5:c.288+12C= ENSP00000440345.1:n.288+12C=
ENST00000595085.5:c.288+12C= ENSP00000471150.2:n.288+12C=
ENST00000604424.1:n.542C=
NM_000709.3:c.288+12C= NP_000700.1:n.288+12C=
NM_001164783.1:c.288+12C= NP_001158255.1:n.288+12C=
NM_000709.4:c.288+12C= MANE Select NP_000700.1:n.288+12C=
NM_001164783.2:c.288+12C= NP_001158255.1:n.288+12C=