Canonical Allele Identifier: CA2336460028
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424462G= , CM000681.2:g.41424462G= GRCh38
NC_000019.9:g.41930367G= , CM000681.1:g.41930367G= GRCh37
NC_000019.8:g.46622207G= NCBI36
NG_013004.1:g.31674G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1192G= MANE Select ENSP00000269980.2:p.Glu398=
ENST00000269980.6:c.1192G= ENSP00000269980.2:p.Glu398=
ENST00000457836.6:c.1201G= ENSP00000416000.2:p.Glu401=
ENST00000540732.3:c.1294G= ENSP00000443246.1:p.Glu432=
ENST00000544905.1:c.62-40G=
ENST00000595085.5:c.922+1765G= ENSP00000471150.2:n.922+1765G=
NM_000709.3:c.1192G= NP_000700.1:p.Glu398=
NM_001164783.1:c.1189G= NP_001158255.1:p.Glu397=
NM_000709.4:c.1192G= MANE Select NP_000700.1:p.Glu398=
NM_001164783.2:c.1189G= NP_001158255.1:p.Glu397=