Canonical Allele Identifier: CA2336460029
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424463A= , CM000681.2:g.41424463A= GRCh38
NC_000019.9:g.41930368A= , CM000681.1:g.41930368A= GRCh37
NC_000019.8:g.46622208A= NCBI36
NG_013004.1:g.31675A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1193A= MANE Select ENSP00000269980.2:p.Glu398=
ENST00000269980.6:c.1193A= ENSP00000269980.2:p.Glu398=
ENST00000457836.6:c.1202A= ENSP00000416000.2:p.Glu401=
ENST00000540732.3:c.1295A= ENSP00000443246.1:p.Glu432=
ENST00000544905.1:c.62-39A=
ENST00000595085.5:c.922+1766A= ENSP00000471150.2:n.922+1766A=
NM_000709.3:c.1193A= NP_000700.1:p.Glu398=
NM_001164783.1:c.1190A= NP_001158255.1:p.Glu397=
NM_000709.4:c.1193A= MANE Select NP_000700.1:p.Glu398=
NM_001164783.2:c.1190A= NP_001158255.1:p.Glu397=