Canonical Allele Identifier: CA2336459198
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422621C= , CM000681.2:g.41422621C= GRCh38
NC_000019.9:g.41928526C= , CM000681.1:g.41928526C= GRCh37
NC_000019.8:g.46620366C= NCBI36
NG_013004.1:g.29833C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.854-8C= MANE Select ENSP00000269980.2:n.854-8C=
ENST00000269980.6:c.854-8C= ENSP00000269980.2:n.854-8C=
ENST00000457836.6:c.788-8C= ENSP00000416000.2:n.788-8C=
ENST00000535632.5:n.483-8C=
ENST00000540732.3:c.956-8C= ENSP00000443246.1:n.956-8C=
ENST00000542943.5:c.767-8C= ENSP00000440345.1:n.767-8C=
ENST00000545787.1:n.482-8C=
ENST00000595085.5:c.854-8C= ENSP00000471150.2:n.854-8C=
NM_000709.3:c.854-8C= NP_000700.1:n.854-8C=
NM_001164783.1:c.854-11C= NP_001158255.1:n.854-11C=
NM_000709.4:c.854-8C= MANE Select NP_000700.1:n.854-8C=
NM_001164783.2:c.854-11C= NP_001158255.1:n.854-11C=