Canonical Allele Identifier: CA2336460062
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424532G= , CM000681.2:g.41424532G= GRCh38
NC_000019.9:g.41930437G= , CM000681.1:g.41930437G= GRCh37
NC_000019.8:g.46622277G= NCBI36
NG_013004.1:g.31744G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1262G= MANE Select ENSP00000269980.2:p.Arg421=
ENST00000269980.6:c.1262G= ENSP00000269980.2:p.Arg421=
ENST00000457836.6:c.1271G= ENSP00000416000.2:p.Arg424=
ENST00000540732.3:c.1364G= ENSP00000443246.1:p.Arg455=
ENST00000544905.1:c.92G=
ENST00000595085.5:c.922+1835G= ENSP00000471150.2:n.922+1835G=
NM_000709.3:c.1262G= NP_000700.1:p.Arg421=
NM_001164783.1:c.1259G= NP_001158255.1:p.Arg420=
NM_000709.4:c.1262G= MANE Select NP_000700.1:p.Arg421=
NM_001164783.2:c.1259G= NP_001158255.1:p.Arg420=