Canonical Allele Identifier: CA2336458884
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41421972C= , CM000681.2:g.41421972C= GRCh38
NC_000019.9:g.41927877C= , CM000681.1:g.41927877C= GRCh37
NC_000019.8:g.46619717C= NCBI36
NG_013004.1:g.29184C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.647-192C= MANE Select ENSP00000269980.2:n.647-192C=
ENST00000269980.6:c.647-192C= ENSP00000269980.2:n.647-192C=
ENST00000457836.6:c.581-192C= ENSP00000416000.2:n.581-192C=
ENST00000535632.5:n.276-192C=
ENST00000538423.5:n.773-192C=
ENST00000540732.3:c.749-192C= ENSP00000443246.1:n.749-192C=
ENST00000541315.1:c.547-192C=
ENST00000542943.5:c.560-192C= ENSP00000440345.1:n.560-192C=
ENST00000545787.1:n.275-192C=
ENST00000595085.5:c.647-192C= ENSP00000471150.2:n.647-192C=
NM_000709.3:c.647-192C= NP_000700.1:n.647-192C=
NM_001164783.1:c.647-192C= NP_001158255.1:n.647-192C=
NM_000709.4:c.647-192C= MANE Select NP_000700.1:n.647-192C=
NM_001164783.2:c.647-192C= NP_001158255.1:n.647-192C=