Canonical Allele Identifier: CA2336453769
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41410665C= , CM000681.2:g.41410665C= GRCh38
NC_000019.9:g.41916570C= , CM000681.1:g.41916570C= GRCh37
NC_000019.8:g.46608410C= NCBI36
NG_013004.1:g.17877C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.137C= MANE Select ENSP00000269980.2:p.Ser46=
ENST00000269980.6:c.137C= ENSP00000269980.2:p.Ser46=
ENST00000457836.6:c.71C= ENSP00000416000.2:p.Ser24=
ENST00000538423.5:n.157C=
ENST00000540732.3:c.239C= ENSP00000443246.1:p.Ser80=
ENST00000542943.5:c.137C= ENSP00000440345.1:p.Ser46=
ENST00000595085.5:c.137C= ENSP00000471150.2:p.Ser46=
ENST00000604424.1:n.379C=
NM_000709.3:c.137C= NP_000700.1:p.Ser46=
NM_001164783.1:c.137C= NP_001158255.1:p.Ser46=
NM_000709.4:c.137C= MANE Select NP_000700.1:p.Ser46=
NM_001164783.2:c.137C= NP_001158255.1:p.Ser46=