Canonical Allele Identifier: CA406004688

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41916616T>G (hg19) ; chr19:g.41410711T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41410711T>G , CM000681.2:g.41410711T>G	GRCh38
NC_000019.9:g.41916616T>G , CM000681.1:g.41916616T>G	GRCh37
NC_000019.8:g.46608456T>G	NCBI36
NG_013004.1:g.17923T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.183T>G MANE Select	ENSP00000269980.2:p.Phe61Leu
ENST00000269980.6:c.183T>G	ENSP00000269980.2:p.Phe61Leu
ENST00000457836.6:c.117T>G	ENSP00000416000.2:p.Phe39Leu
ENST00000538423.5:n.203T>G
ENST00000540732.3:c.285T>G	ENSP00000443246.1:p.Phe95Leu
ENST00000542943.5:c.183T>G	ENSP00000440345.1:p.Phe61Leu
ENST00000595085.5:c.183T>G	ENSP00000471150.2:p.Phe61Leu
ENST00000604424.1:n.425T>G
NM_000709.3:c.183T>G	NP_000700.1:p.Phe61Leu
NM_001164783.1:c.183T>G	NP_001158255.1:p.Phe61Leu
NM_000709.4:c.183T>G MANE Select	NP_000700.1:p.Phe61Leu
NM_001164783.2:c.183T>G	NP_001158255.1:p.Phe61Leu