Canonical Allele Identifier: CA2336458946
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422107T= , CM000681.2:g.41422107T= GRCh38
NC_000019.9:g.41928012T= , CM000681.1:g.41928012T= GRCh37
NC_000019.8:g.46619852T= NCBI36
NG_013004.1:g.29319T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.647-57T= MANE Select ENSP00000269980.2:n.647-57T=
ENST00000269980.6:c.647-57T= ENSP00000269980.2:n.647-57T=
ENST00000457836.6:c.581-57T= ENSP00000416000.2:n.581-57T=
ENST00000535632.5:n.276-57T=
ENST00000538423.5:n.773-57T=
ENST00000540732.3:c.749-57T= ENSP00000443246.1:n.749-57T=
ENST00000541315.1:c.547-57T=
ENST00000542943.5:c.560-57T= ENSP00000440345.1:n.560-57T=
ENST00000545787.1:n.275-57T=
ENST00000595085.5:c.647-57T= ENSP00000471150.2:n.647-57T=
NM_000709.3:c.647-57T= NP_000700.1:n.647-57T=
NM_001164783.1:c.647-57T= NP_001158255.1:n.647-57T=
NM_000709.4:c.647-57T= MANE Select NP_000700.1:n.647-57T=
NM_001164783.2:c.647-57T= NP_001158255.1:n.647-57T=