Canonical Allele Identifier: CA406015744

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41930494T>G (hg19) ; chr19:g.41424589T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41424589T>G , CM000681.2:g.41424589T>G	GRCh38
NC_000019.9:g.41930494T>G , CM000681.1:g.41930494T>G	GRCh37
NC_000019.8:g.46622334T>G	NCBI36
NG_013004.1:g.31801T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269980.7:c.1319T>G MANE Select	ENSP00000269980.2:p.Leu440Arg
ENST00000269980.6:c.1319T>G	ENSP00000269980.2:p.Leu440Arg
ENST00000457836.6:c.1328T>G	ENSP00000416000.2:p.Leu443Arg
ENST00000540732.3:c.1421T>G	ENSP00000443246.1:p.Leu474Arg
ENST00000544905.1:c.149T>G
ENST00000595085.5:c.922+1892T>G	ENSP00000471150.2:n.922+1892T>G
NM_000709.3:c.1319T>G	NP_000700.1:p.Leu440Arg
NM_001164783.1:c.1316T>G	NP_001158255.1:p.Leu439Arg
NM_000709.4:c.1319T>G MANE Select	NP_000700.1:p.Leu440Arg
NM_001164783.2:c.1316T>G	NP_001158255.1:p.Leu439Arg