Canonical Allele Identifier: CA2336459112
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422421T= , CM000681.2:g.41422421T= GRCh38
NC_000019.9:g.41928326T= , CM000681.1:g.41928326T= GRCh37
NC_000019.8:g.46620166T= NCBI36
NG_013004.1:g.29633T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.853+51T= MANE Select ENSP00000269980.2:n.853+51T=
ENST00000269980.6:c.853+51T= ENSP00000269980.2:n.853+51T=
ENST00000457836.6:c.787+51T= ENSP00000416000.2:n.787+51T=
ENST00000535632.5:n.482+51T=
ENST00000540732.3:c.955+51T= ENSP00000443246.1:n.955+51T=
ENST00000542943.5:c.766+51T= ENSP00000440345.1:n.766+51T=
ENST00000545787.1:n.481+51T=
ENST00000595085.5:c.853+51T= ENSP00000471150.2:n.853+51T=
NM_000709.3:c.853+51T= NP_000700.1:n.853+51T=
NM_001164783.1:c.853+51T= NP_001158255.1:n.853+51T=
NM_000709.4:c.853+51T= MANE Select NP_000700.1:n.853+51T=
NM_001164783.2:c.853+51T= NP_001158255.1:n.853+51T=