Canonical Allele Identifier: CA406012667

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928074G>A (hg19) ; chr19:g.41422169G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422169G>A , CM000681.2:g.41422169G>A	GRCh38
NC_000019.9:g.41928074G>A , CM000681.1:g.41928074G>A	GRCh37
NC_000019.8:g.46619914G>A	NCBI36
NG_013004.1:g.29381G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269980.7:c.652G>A MANE Select	ENSP00000269980.2:p.Gly218Arg
ENST00000269980.6:c.652G>A	ENSP00000269980.2:p.Gly218Arg
ENST00000457836.6:c.586G>A	ENSP00000416000.2:p.Gly196Arg
ENST00000535632.5:n.281G>A
ENST00000538423.5:n.778G>A
ENST00000540732.3:c.754G>A	ENSP00000443246.1:p.Gly252Arg
ENST00000541315.1:c.552G>A
ENST00000542943.5:c.565G>A	ENSP00000440345.1:p.Gly189Arg
ENST00000545787.1:n.280G>A
ENST00000595085.5:c.652G>A	ENSP00000471150.2:p.Gly218Arg
NM_000709.3:c.652G>A	NP_000700.1:p.Gly218Arg
NM_001164783.1:c.652G>A	NP_001158255.1:p.Gly218Arg
NM_000709.4:c.652G>A MANE Select	NP_000700.1:p.Gly218Arg
NM_001164783.2:c.652G>A	NP_001158255.1:p.Gly218Arg