Canonical Allele Identifier: CA406013399

Gene: BCKDHA

Linked Data

• gnomAD v4: 19-41422696-C-G
• MyVariant Identifiers: chr19:g.41928601C>G (hg19) ; chr19:g.41422696C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422696C>G , CM000681.2:g.41422696C>G	GRCh38
NC_000019.9:g.41928601C>G , CM000681.1:g.41928601C>G	GRCh37
NC_000019.8:g.46620441C>G	NCBI36
NG_013004.1:g.29908C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.921C>G MANE Select	ENSP00000269980.2:p.Tyr307Ter
ENST00000269980.6:c.921C>G	ENSP00000269980.2:p.Tyr307Ter
ENST00000457836.6:c.855C>G	ENSP00000416000.2:p.Tyr285Ter
ENST00000535632.5:n.550C>G
ENST00000540732.3:c.1023C>G	ENSP00000443246.1:p.Tyr341Ter
ENST00000542943.5:c.834C>G	ENSP00000440345.1:p.Tyr278Ter
ENST00000545787.1:n.549C>G
ENST00000595085.5:c.921C>G	ENSP00000471150.2:p.Tyr307Ter
NM_000709.3:c.921C>G	NP_000700.1:p.Tyr307Ter
NM_001164783.1:c.918C>G	NP_001158255.1:p.Tyr306Ter
NM_000709.4:c.921C>G MANE Select	NP_000700.1:p.Tyr307Ter
NM_001164783.2:c.918C>G	NP_001158255.1:p.Tyr306Ter