Canonical Allele Identifier: CA406015771

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41930498T>G (hg19) ; chr19:g.41424593T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41424593T>G , CM000681.2:g.41424593T>G	GRCh38
NC_000019.9:g.41930498T>G , CM000681.1:g.41930498T>G	GRCh37
NC_000019.8:g.46622338T>G	NCBI36
NG_013004.1:g.31805T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1323T>G MANE Select	ENSP00000269980.2:p.Asp441Glu
ENST00000269980.6:c.1323T>G	ENSP00000269980.2:p.Asp441Glu
ENST00000457836.6:c.1332T>G	ENSP00000416000.2:p.Asp444Glu
ENST00000540732.3:c.1425T>G	ENSP00000443246.1:p.Asp475Glu
ENST00000544905.1:c.153T>G
ENST00000595085.5:c.922+1896T>G	ENSP00000471150.2:n.922+1896T>G
NM_000709.3:c.1323T>G	NP_000700.1:p.Asp441Glu
NM_001164783.1:c.1320T>G	NP_001158255.1:p.Asp440Glu
NM_000709.4:c.1323T>G MANE Select	NP_000700.1:p.Asp441Glu
NM_001164783.2:c.1320T>G	NP_001158255.1:p.Asp440Glu