Canonical Allele Identifier: CA2336460034
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424478C= , CM000681.2:g.41424478C= GRCh38
NC_000019.9:g.41930383C= , CM000681.1:g.41930383C= GRCh37
NC_000019.8:g.46622223C= NCBI36
NG_013004.1:g.31690C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1208C= MANE Select ENSP00000269980.2:p.Pro403=
ENST00000269980.6:c.1208C= ENSP00000269980.2:p.Pro403=
ENST00000457836.6:c.1217C= ENSP00000416000.2:p.Pro406=
ENST00000540732.3:c.1310C= ENSP00000443246.1:p.Pro437=
ENST00000544905.1:c.62-24C=
ENST00000595085.5:c.922+1781C= ENSP00000471150.2:n.922+1781C=
NM_000709.3:c.1208C= NP_000700.1:p.Pro403=
NM_001164783.1:c.1205C= NP_001158255.1:p.Pro402=
NM_000709.4:c.1208C= MANE Select NP_000700.1:p.Pro403=
NM_001164783.2:c.1205C= NP_001158255.1:p.Pro402=