Canonical Allele Identifier: CA2336459091
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422387C= , CM000681.2:g.41422387C= GRCh38
NC_000019.9:g.41928292C= , CM000681.1:g.41928292C= GRCh37
NC_000019.8:g.46620132C= NCBI36
NG_013004.1:g.29599C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.853+17C= MANE Select ENSP00000269980.2:n.853+17C=
ENST00000269980.6:c.853+17C= ENSP00000269980.2:n.853+17C=
ENST00000457836.6:c.787+17C= ENSP00000416000.2:n.787+17C=
ENST00000535632.5:n.482+17C=
ENST00000540732.3:c.955+17C= ENSP00000443246.1:n.955+17C=
ENST00000542943.5:c.766+17C= ENSP00000440345.1:n.766+17C=
ENST00000545787.1:n.481+17C=
ENST00000595085.5:c.853+17C= ENSP00000471150.2:n.853+17C=
NM_000709.3:c.853+17C= NP_000700.1:n.853+17C=
NM_001164783.1:c.853+17C= NP_001158255.1:n.853+17C=
NM_000709.4:c.853+17C= MANE Select NP_000700.1:n.853+17C=
NM_001164783.2:c.853+17C= NP_001158255.1:n.853+17C=