Canonical Allele Identifier: CA406004725

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41916632T>A (hg19) ; chr19:g.41410727T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41410727T>A , CM000681.2:g.41410727T>A	GRCh38
NC_000019.9:g.41916632T>A , CM000681.1:g.41916632T>A	GRCh37
NC_000019.8:g.46608472T>A	NCBI36
NG_013004.1:g.17939T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.199T>A MANE Select	ENSP00000269980.2:p.Phe67Ile
ENST00000269980.6:c.199T>A	ENSP00000269980.2:p.Phe67Ile
ENST00000457836.6:c.133T>A	ENSP00000416000.2:p.Phe45Ile
ENST00000538423.5:n.219T>A
ENST00000540732.3:c.301T>A	ENSP00000443246.1:p.Phe101Ile
ENST00000541315.1:c.6T>A
ENST00000542943.5:c.199T>A	ENSP00000440345.1:p.Phe67Ile
ENST00000595085.5:c.199T>A	ENSP00000471150.2:p.Phe67Ile
ENST00000604424.1:n.441T>A
NM_000709.3:c.199T>A	NP_000700.1:p.Phe67Ile
NM_001164783.1:c.199T>A	NP_001158255.1:p.Phe67Ile
NM_000709.4:c.199T>A MANE Select	NP_000700.1:p.Phe67Ile
NM_001164783.2:c.199T>A	NP_001158255.1:p.Phe67Ile