Canonical Allele Identifier: CA406015813

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41930503T>A (hg19) ; chr19:g.41424598T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41424598T>A , CM000681.2:g.41424598T>A	GRCh38
NC_000019.9:g.41930503T>A , CM000681.1:g.41930503T>A	GRCh37
NC_000019.8:g.46622343T>A	NCBI36
NG_013004.1:g.31810T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1328T>A MANE Select	ENSP00000269980.2:p.Phe443Tyr
ENST00000269980.6:c.1328T>A	ENSP00000269980.2:p.Phe443Tyr
ENST00000457836.6:c.1337T>A	ENSP00000416000.2:p.Phe446Tyr
ENST00000540732.3:c.1430T>A	ENSP00000443246.1:p.Phe477Tyr
ENST00000544905.1:c.158T>A
ENST00000595085.5:c.922+1901T>A	ENSP00000471150.2:n.922+1901T>A
NM_000709.3:c.1328T>A	NP_000700.1:p.Phe443Tyr
NM_001164783.1:c.1325T>A	NP_001158255.1:p.Phe442Tyr
NM_000709.4:c.1328T>A MANE Select	NP_000700.1:p.Phe443Tyr
NM_001164783.2:c.1325T>A	NP_001158255.1:p.Phe442Tyr