Canonical Allele Identifier: CA406004890
Gene: BCKDHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41410776A>C , CM000681.2:g.41410776A>C GRCh38
NC_000019.9:g.41916681A>C , CM000681.1:g.41916681A>C GRCh37
NC_000019.8:g.46608521A>C NCBI36
NG_013004.1:g.17988A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.248A>C MANE Select ENSP00000269980.2:p.Asp83Ala
ENST00000269980.6:c.248A>C ENSP00000269980.2:p.Asp83Ala
ENST00000457836.6:c.182A>C ENSP00000416000.2:p.Asp61Ala
ENST00000538423.5:n.268A>C
ENST00000540732.3:c.350A>C ENSP00000443246.1:p.Asp117Ala
ENST00000541315.1:c.55A>C
ENST00000542943.5:c.248A>C ENSP00000440345.1:p.Asp83Ala
ENST00000595085.5:c.248A>C ENSP00000471150.2:p.Asp83Ala
ENST00000604424.1:n.490A>C
NM_000709.3:c.248A>C NP_000700.1:p.Asp83Ala
NM_001164783.1:c.248A>C NP_001158255.1:p.Asp83Ala
NM_000709.4:c.248A>C MANE Select NP_000700.1:p.Asp83Ala
NM_001164783.2:c.248A>C NP_001158255.1:p.Asp83Ala