Canonical Allele Identifier: CA2336459032
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422262G= , CM000681.2:g.41422262G= GRCh38
NC_000019.9:g.41928167G= , CM000681.1:g.41928167G= GRCh37
NC_000019.8:g.46620007G= NCBI36
NG_013004.1:g.29474G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.745G= MANE Select ENSP00000269980.2:p.Gly249=
ENST00000269980.6:c.745G= ENSP00000269980.2:p.Gly249=
ENST00000457836.6:c.679G= ENSP00000416000.2:p.Gly227=
ENST00000535632.5:n.374G=
ENST00000540732.3:c.847G= ENSP00000443246.1:p.Gly283=
ENST00000542943.5:c.658G= ENSP00000440345.1:p.Gly220=
ENST00000545787.1:n.373G=
ENST00000595085.5:c.745G= ENSP00000471150.2:p.Gly249=
NM_000709.3:c.745G= NP_000700.1:p.Gly249=
NM_001164783.1:c.745G= NP_001158255.1:p.Gly249=
NM_000709.4:c.745G= MANE Select NP_000700.1:p.Gly249=
NM_001164783.2:c.745G= NP_001158255.1:p.Gly249=