Canonical Allele Identifier: CA2336459063
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422325G= , CM000681.2:g.41422325G= GRCh38
NC_000019.9:g.41928230G= , CM000681.1:g.41928230G= GRCh37
NC_000019.8:g.46620070G= NCBI36
NG_013004.1:g.29537G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.808G= MANE Select ENSP00000269980.2:p.Ala270=
ENST00000269980.6:c.808G= ENSP00000269980.2:p.Ala270=
ENST00000457836.6:c.742G= ENSP00000416000.2:p.Ala248=
ENST00000535632.5:n.437G=
ENST00000540732.3:c.910G= ENSP00000443246.1:p.Ala304=
ENST00000542943.5:c.721G= ENSP00000440345.1:p.Ala241=
ENST00000545787.1:n.436G=
ENST00000595085.5:c.808G= ENSP00000471150.2:p.Ala270=
NM_000709.3:c.808G= NP_000700.1:p.Ala270=
NM_001164783.1:c.808G= NP_001158255.1:p.Ala270=
NM_000709.4:c.808G= MANE Select NP_000700.1:p.Ala270=
NM_001164783.2:c.808G= NP_001158255.1:p.Ala270=