Canonical Allele Identifier: CA2838273729
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41408598A>G , CM000681.2:g.41408598A>G GRCh38
NC_000019.9:g.41914503A>G , CM000681.1:g.41914503A>G GRCh37
NC_000019.8:g.46606343A>G NCBI36
NG_013004.1:g.15810A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.109-2039A>G MANE Select ENSP00000269980.2:n.109-2039A>G
ENST00000269980.6:c.109-2039A>G ENSP00000269980.2:n.109-2039A>G
ENST00000457836.6:c.58-2054A>G ENSP00000416000.2:n.58-2054A>G
ENST00000538423.5:n.129-2039A>G
ENST00000540732.3:c.211-2039A>G ENSP00000443246.1:n.211-2039A>G
ENST00000542943.5:c.109-2039A>G ENSP00000440345.1:n.109-2039A>G
ENST00000595085.5:c.109-2039A>G ENSP00000471150.2:n.109-2039A>G
ENST00000604424.1:n.351-2039A>G
NM_000709.3:c.109-2039A>G NP_000700.1:n.109-2039A>G
NM_001164783.1:c.109-2039A>G NP_001158255.1:n.109-2039A>G
NM_000709.4:c.109-2039A>G MANE Select NP_000700.1:n.109-2039A>G
NM_001164783.2:c.109-2039A>G NP_001158255.1:n.109-2039A>G