Canonical Allele Identifier: CA406012682

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928083T>G (hg19) ; chr19:g.41422178T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422178T>G , CM000681.2:g.41422178T>G	GRCh38
NC_000019.9:g.41928083T>G , CM000681.1:g.41928083T>G	GRCh37
NC_000019.8:g.46619923T>G	NCBI36
NG_013004.1:g.29390T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269980.7:c.661T>G MANE Select	ENSP00000269980.2:p.Tyr221Asp
ENST00000269980.6:c.661T>G	ENSP00000269980.2:p.Tyr221Asp
ENST00000457836.6:c.595T>G	ENSP00000416000.2:p.Tyr199Asp
ENST00000535632.5:n.290T>G
ENST00000538423.5:n.787T>G
ENST00000540732.3:c.763T>G	ENSP00000443246.1:p.Tyr255Asp
ENST00000541315.1:c.561T>G
ENST00000542943.5:c.574T>G	ENSP00000440345.1:p.Tyr192Asp
ENST00000545787.1:n.289T>G
ENST00000595085.5:c.661T>G	ENSP00000471150.2:p.Tyr221Asp
NM_000709.3:c.661T>G	NP_000700.1:p.Tyr221Asp
NM_001164783.1:c.661T>G	NP_001158255.1:p.Tyr221Asp
NM_000709.4:c.661T>G MANE Select	NP_000700.1:p.Tyr221Asp
NM_001164783.2:c.661T>G	NP_001158255.1:p.Tyr221Asp