Canonical Allele Identifier: CA2336459409
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41423038C= , CM000681.2:g.41423038C= GRCh38
NC_000019.9:g.41928943C= , CM000681.1:g.41928943C= GRCh37
NC_000019.8:g.46620783C= NCBI36
NG_013004.1:g.30250C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1036C= MANE Select ENSP00000269980.2:p.Arg346=
ENST00000269980.6:c.1036C= ENSP00000269980.2:p.Arg346=
ENST00000457836.6:c.1045C= ENSP00000416000.2:p.Arg349=
ENST00000540732.3:c.1138C= ENSP00000443246.1:p.Arg380=
ENST00000542943.5:c.949C= ENSP00000440345.1:p.Arg317=
ENST00000595085.5:c.922+341C= ENSP00000471150.2:n.922+341C=
NM_000709.3:c.1036C= NP_000700.1:p.Arg346=
NM_001164783.1:c.1033C= NP_001158255.1:p.Arg345=
NM_000709.4:c.1036C= MANE Select NP_000700.1:p.Arg346=
NM_001164783.2:c.1033C= NP_001158255.1:p.Arg345=