Canonical Allele Identifier: CA406004737

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41916637C>G (hg19) ; chr19:g.41410732C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41410732C>G , CM000681.2:g.41410732C>G	GRCh38
NC_000019.9:g.41916637C>G , CM000681.1:g.41916637C>G	GRCh37
NC_000019.8:g.46608477C>G	NCBI36
NG_013004.1:g.17944C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.204C>G MANE Select	ENSP00000269980.2:p.Ile68Met
ENST00000269980.6:c.204C>G	ENSP00000269980.2:p.Ile68Met
ENST00000457836.6:c.138C>G	ENSP00000416000.2:p.Ile46Met
ENST00000538423.5:n.224C>G
ENST00000540732.3:c.306C>G	ENSP00000443246.1:p.Ile102Met
ENST00000541315.1:c.11C>G
ENST00000542943.5:c.204C>G	ENSP00000440345.1:p.Ile68Met
ENST00000595085.5:c.204C>G	ENSP00000471150.2:p.Ile68Met
ENST00000604424.1:n.446C>G
NM_000709.3:c.204C>G	NP_000700.1:p.Ile68Met
NM_001164783.1:c.204C>G	NP_001158255.1:p.Ile68Met
NM_000709.4:c.204C>G MANE Select	NP_000700.1:p.Ile68Met
NM_001164783.2:c.204C>G	NP_001158255.1:p.Ile68Met