Canonical Allele Identifier: CA507690678

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928547C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422642C>A , CM000681.2:g.41422642C>A	GRCh38
NC_000019.9:g.41928547C>A , CM000681.1:g.41928547C>A	GRCh37
NC_000019.8:g.46620387C>A	NCBI36
NG_013004.1:g.29854C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269980.7:c.867C>A MANE Select	ENSP00000269980.2:p.Pro289=
ENST00000269980.6:c.867C>A	ENSP00000269980.2:p.Pro289=
ENST00000457836.6:c.801C>A	ENSP00000416000.2:p.Pro267=
ENST00000535632.5:n.496C>A
ENST00000540732.3:c.969C>A	ENSP00000443246.1:p.Pro323=
ENST00000542943.5:c.780C>A	ENSP00000440345.1:p.Pro260=
ENST00000545787.1:n.495C>A
ENST00000595085.5:c.867C>A	ENSP00000471150.2:p.Pro289=
NM_000709.3:c.867C>A	NP_000700.1:p.Pro289=
NM_001164783.1:c.864C>A	NP_001158255.1:p.Pro288=
NM_000709.4:c.867C>A MANE Select	NP_000700.1:p.Pro289=
NM_001164783.2:c.864C>A	NP_001158255.1:p.Pro288=