Canonical Allele Identifier: CA2336453793
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41410719A= , CM000681.2:g.41410719A= GRCh38
NC_000019.9:g.41916624A= , CM000681.1:g.41916624A= GRCh37
NC_000019.8:g.46608464A= NCBI36
NG_013004.1:g.17931A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.191A= MANE Select ENSP00000269980.2:p.Lys64=
ENST00000269980.6:c.191A= ENSP00000269980.2:p.Lys64=
ENST00000457836.6:c.125A= ENSP00000416000.2:p.Lys42=
ENST00000538423.5:n.211A=
ENST00000540732.3:c.293A= ENSP00000443246.1:p.Lys98=
ENST00000542943.5:c.191A= ENSP00000440345.1:p.Lys64=
ENST00000595085.5:c.191A= ENSP00000471150.2:p.Lys64=
ENST00000604424.1:n.433A=
NM_000709.3:c.191A= NP_000700.1:p.Lys64=
NM_001164783.1:c.191A= NP_001158255.1:p.Lys64=
NM_000709.4:c.191A= MANE Select NP_000700.1:p.Lys64=
NM_001164783.2:c.191A= NP_001158255.1:p.Lys64=