Canonical Allele Identifier: CA406013439

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928620C>G (hg19) ; chr19:g.41422715C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422715C>G , CM000681.2:g.41422715C>G	GRCh38
NC_000019.9:g.41928620C>G , CM000681.1:g.41928620C>G	GRCh37
NC_000019.8:g.46620460C>G	NCBI36
NG_013004.1:g.29927C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269980.7:c.940C>G MANE Select	ENSP00000269980.2:p.Arg314Gly
ENST00000269980.6:c.940C>G	ENSP00000269980.2:p.Arg314Gly
ENST00000457836.6:c.874C>G	ENSP00000416000.2:p.Arg292Gly
ENST00000535632.5:n.569C>G
ENST00000540732.3:c.1042C>G	ENSP00000443246.1:p.Arg348Gly
ENST00000542943.5:c.853C>G	ENSP00000440345.1:p.Arg285Gly
ENST00000545787.1:n.568C>G
ENST00000595085.5:c.922+18C>G	ENSP00000471150.2:n.922+18C>G
NM_000709.3:c.940C>G	NP_000700.1:p.Arg314Gly
NM_001164783.1:c.937C>G	NP_001158255.1:p.Arg313Gly
NM_000709.4:c.940C>G MANE Select	NP_000700.1:p.Arg314Gly
NM_001164783.2:c.937C>G	NP_001158255.1:p.Arg313Gly