Canonical Allele Identifier: CA406012879

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928176T>C (hg19) ; chr19:g.41422271T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422271T>C , CM000681.2:g.41422271T>C	GRCh38
NC_000019.9:g.41928176T>C , CM000681.1:g.41928176T>C	GRCh37
NC_000019.8:g.46620016T>C	NCBI36
NG_013004.1:g.29483T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000269980.7:c.754T>C MANE Select	ENSP00000269980.2:p.Phe252Leu
ENST00000269980.6:c.754T>C	ENSP00000269980.2:p.Phe252Leu
ENST00000457836.6:c.688T>C	ENSP00000416000.2:p.Phe230Leu
ENST00000535632.5:n.383T>C
ENST00000540732.3:c.856T>C	ENSP00000443246.1:p.Phe286Leu
ENST00000542943.5:c.667T>C	ENSP00000440345.1:p.Phe223Leu
ENST00000545787.1:n.382T>C
ENST00000595085.5:c.754T>C	ENSP00000471150.2:p.Phe252Leu
NM_000709.3:c.754T>C	NP_000700.1:p.Phe252Leu
NM_001164783.1:c.754T>C	NP_001158255.1:p.Phe252Leu
NM_000709.4:c.754T>C MANE Select	NP_000700.1:p.Phe252Leu
NM_001164783.2:c.754T>C	NP_001158255.1:p.Phe252Leu