Canonical Allele Identifier: CA2336458993
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422190C= , CM000681.2:g.41422190C= GRCh38
NC_000019.9:g.41928095C= , CM000681.1:g.41928095C= GRCh37
NC_000019.8:g.46619935C= NCBI36
NG_013004.1:g.29402C=

Transcript Alleles

HGVS Amino-acid change
ENST00000269980.7:c.673C= MANE Select ENSP00000269980.2:p.Arg225=
ENST00000269980.6:c.673C= ENSP00000269980.2:p.Arg225=
ENST00000457836.6:c.607C= ENSP00000416000.2:p.Arg203=
ENST00000535632.5:n.302C=
ENST00000538423.5:n.799C=
ENST00000540732.3:c.775C= ENSP00000443246.1:p.Arg259=
ENST00000541315.1:c.573C=
ENST00000542943.5:c.586C= ENSP00000440345.1:p.Arg196=
ENST00000545787.1:n.301C=
ENST00000595085.5:c.673C= ENSP00000471150.2:p.Arg225=
NM_000709.3:c.673C= NP_000700.1:p.Arg225=
NM_001164783.1:c.673C= NP_001158255.1:p.Arg225=
NM_000709.4:c.673C= MANE Select NP_000700.1:p.Arg225=
NM_001164783.2:c.673C= NP_001158255.1:p.Arg225=