Canonical Allele Identifier: CA2336460026
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424459G= , CM000681.2:g.41424459G= GRCh38
NC_000019.9:g.41930364G= , CM000681.1:g.41930364G= GRCh37
NC_000019.8:g.46622204G= NCBI36
NG_013004.1:g.31671G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1189G= MANE Select ENSP00000269980.2:p.Ala397=
ENST00000269980.6:c.1189G= ENSP00000269980.2:p.Ala397=
ENST00000457836.6:c.1198G= ENSP00000416000.2:p.Ala400=
ENST00000540732.3:c.1291G= ENSP00000443246.1:p.Ala431=
ENST00000544905.1:c.62-43G=
ENST00000595085.5:c.922+1762G= ENSP00000471150.2:n.922+1762G=
NM_000709.3:c.1189G= NP_000700.1:p.Ala397=
NM_001164783.1:c.1186G= NP_001158255.1:p.Ala396=
NM_000709.4:c.1189G= MANE Select NP_000700.1:p.Ala397=
NM_001164783.2:c.1186G= NP_001158255.1:p.Ala396=