Canonical Allele Identifier: CA2336453978
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41411032G= , CM000681.2:g.41411032G= GRCh38
NC_000019.9:g.41916937G= , CM000681.1:g.41916937G= GRCh37
NC_000019.8:g.46608777G= NCBI36
NG_013004.1:g.18244G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.375+23G= MANE Select ENSP00000269980.2:n.375+23G=
ENST00000269980.6:c.375+23G= ENSP00000269980.2:n.375+23G=
ENST00000457836.6:c.309+23G= ENSP00000416000.2:n.309+23G=
ENST00000538423.5:n.501+23G=
ENST00000540732.3:c.477+23G= ENSP00000443246.1:n.477+23G=
ENST00000541315.1:c.182+23G=
ENST00000542943.5:c.288+216G= ENSP00000440345.1:n.288+216G=
ENST00000595085.5:c.375+23G= ENSP00000471150.2:n.375+23G=
NM_000709.3:c.375+23G= NP_000700.1:n.375+23G=
NM_001164783.1:c.375+23G= NP_001158255.1:n.375+23G=
NM_000709.4:c.375+23G= MANE Select NP_000700.1:n.375+23G=
NM_001164783.2:c.375+23G= NP_001158255.1:n.375+23G=