Canonical Allele Identifier: CA406004844
Gene: BCKDHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41410767G>T , CM000681.2:g.41410767G>T GRCh38
NC_000019.9:g.41916672G>T , CM000681.1:g.41916672G>T GRCh37
NC_000019.8:g.46608512G>T NCBI36
NG_013004.1:g.17979G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.239G>T MANE Select ENSP00000269980.2:p.Arg80Leu
ENST00000269980.6:c.239G>T ENSP00000269980.2:p.Arg80Leu
ENST00000457836.6:c.173G>T ENSP00000416000.2:p.Arg58Leu
ENST00000538423.5:n.259G>T
ENST00000540732.3:c.341G>T ENSP00000443246.1:p.Arg114Leu
ENST00000541315.1:c.46G>T
ENST00000542943.5:c.239G>T ENSP00000440345.1:p.Arg80Leu
ENST00000595085.5:c.239G>T ENSP00000471150.2:p.Arg80Leu
ENST00000604424.1:n.481G>T
NM_000709.3:c.239G>T NP_000700.1:p.Arg80Leu
NM_001164783.1:c.239G>T NP_001158255.1:p.Arg80Leu
NM_000709.4:c.239G>T MANE Select NP_000700.1:p.Arg80Leu
NM_001164783.2:c.239G>T NP_001158255.1:p.Arg80Leu