Canonical Allele Identifier: CA406012777

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928129T>A (hg19) ; chr19:g.41422224T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422224T>A , CM000681.2:g.41422224T>A	GRCh38
NC_000019.9:g.41928129T>A , CM000681.1:g.41928129T>A	GRCh37
NC_000019.8:g.46619969T>A	NCBI36
NG_013004.1:g.29436T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.707T>A MANE Select	ENSP00000269980.2:p.Phe236Tyr
ENST00000269980.6:c.707T>A	ENSP00000269980.2:p.Phe236Tyr
ENST00000457836.6:c.641T>A	ENSP00000416000.2:p.Phe214Tyr
ENST00000535632.5:n.336T>A
ENST00000540732.3:c.809T>A	ENSP00000443246.1:p.Phe270Tyr
ENST00000541315.1:c.607T>A
ENST00000542943.5:c.620T>A	ENSP00000440345.1:p.Phe207Tyr
ENST00000545787.1:n.335T>A
ENST00000595085.5:c.707T>A	ENSP00000471150.2:p.Phe236Tyr
NM_000709.3:c.707T>A	NP_000700.1:p.Phe236Tyr
NM_001164783.1:c.707T>A	NP_001158255.1:p.Phe236Tyr
NM_000709.4:c.707T>A MANE Select	NP_000700.1:p.Phe236Tyr
NM_001164783.2:c.707T>A	NP_001158255.1:p.Phe236Tyr