Canonical Allele Identifier: CA406013738

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928904A>T (hg19) ; chr19:g.41422999A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422999A>T , CM000681.2:g.41422999A>T	GRCh38
NC_000019.9:g.41928904A>T , CM000681.1:g.41928904A>T	GRCh37
NC_000019.8:g.46620744A>T	NCBI36
NG_013004.1:g.30211A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.997A>T MANE Select	ENSP00000269980.2:p.Ile333Phe
ENST00000269980.6:c.997A>T	ENSP00000269980.2:p.Ile333Phe
ENST00000457836.6:c.1006A>T	ENSP00000416000.2:p.Ile336Phe
ENST00000540732.3:c.1099A>T	ENSP00000443246.1:p.Ile367Phe
ENST00000542943.5:c.910A>T	ENSP00000440345.1:p.Ile304Phe
ENST00000595085.5:c.922+302A>T	ENSP00000471150.2:n.922+302A>T
NM_000709.3:c.997A>T	NP_000700.1:p.Ile333Phe
NM_001164783.1:c.994A>T	NP_001158255.1:p.Ile332Phe
NM_000709.4:c.997A>T MANE Select	NP_000700.1:p.Ile333Phe
NM_001164783.2:c.994A>T	NP_001158255.1:p.Ile332Phe