Canonical Allele Identifier: CA406013254

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928551T>G (hg19) ; chr19:g.41422646T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422646T>G , CM000681.2:g.41422646T>G	GRCh38
NC_000019.9:g.41928551T>G , CM000681.1:g.41928551T>G	GRCh37
NC_000019.8:g.46620391T>G	NCBI36
NG_013004.1:g.29858T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269980.7:c.871T>G MANE Select	ENSP00000269980.2:p.Tyr291Asp
ENST00000269980.6:c.871T>G	ENSP00000269980.2:p.Tyr291Asp
ENST00000457836.6:c.805T>G	ENSP00000416000.2:p.Tyr269Asp
ENST00000535632.5:n.500T>G
ENST00000540732.3:c.973T>G	ENSP00000443246.1:p.Tyr325Asp
ENST00000542943.5:c.784T>G	ENSP00000440345.1:p.Tyr262Asp
ENST00000545787.1:n.499T>G
ENST00000595085.5:c.871T>G	ENSP00000471150.2:p.Tyr291Asp
NM_000709.3:c.871T>G	NP_000700.1:p.Tyr291Asp
NM_001164783.1:c.868T>G	NP_001158255.1:p.Tyr290Asp
NM_000709.4:c.871T>G MANE Select	NP_000700.1:p.Tyr291Asp
NM_001164783.2:c.868T>G	NP_001158255.1:p.Tyr290Asp