Canonical Allele Identifier: CA406015465

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41930434T>G (hg19) ; chr19:g.41424529T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41424529T>G , CM000681.2:g.41424529T>G	GRCh38
NC_000019.9:g.41930434T>G , CM000681.1:g.41930434T>G	GRCh37
NC_000019.8:g.46622274T>G	NCBI36
NG_013004.1:g.31741T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1259T>G MANE Select	ENSP00000269980.2:p.Leu420Arg
ENST00000269980.6:c.1259T>G	ENSP00000269980.2:p.Leu420Arg
ENST00000457836.6:c.1268T>G	ENSP00000416000.2:p.Leu423Arg
ENST00000540732.3:c.1361T>G	ENSP00000443246.1:p.Leu454Arg
ENST00000544905.1:c.89T>G
ENST00000595085.5:c.922+1832T>G	ENSP00000471150.2:n.922+1832T>G
NM_000709.3:c.1259T>G	NP_000700.1:p.Leu420Arg
NM_001164783.1:c.1256T>G	NP_001158255.1:p.Leu419Arg
NM_000709.4:c.1259T>G MANE Select	NP_000700.1:p.Leu420Arg
NM_001164783.2:c.1256T>G	NP_001158255.1:p.Leu419Arg