Canonical Allele Identifier: CA406013487

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928647C>G (hg19) ; chr19:g.41422742C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422742C>G , CM000681.2:g.41422742C>G	GRCh38
NC_000019.9:g.41928647C>G , CM000681.1:g.41928647C>G	GRCh37
NC_000019.8:g.46620487C>G	NCBI36
NG_013004.1:g.29954C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.967C>G MANE Select	ENSP00000269980.2:p.Pro323Ala
ENST00000269980.6:c.967C>G	ENSP00000269980.2:p.Pro323Ala
ENST00000457836.6:c.901C>G	ENSP00000416000.2:p.Pro301Ala
ENST00000535632.5:n.596C>G
ENST00000540732.3:c.1069C>G	ENSP00000443246.1:p.Pro357Ala
ENST00000542943.5:c.880C>G	ENSP00000440345.1:p.Pro294Ala
ENST00000595085.5:c.922+45C>G	ENSP00000471150.2:n.922+45C>G
NM_000709.3:c.967C>G	NP_000700.1:p.Pro323Ala
NM_001164783.1:c.964C>G	NP_001158255.1:p.Pro322Ala
NM_000709.4:c.967C>G MANE Select	NP_000700.1:p.Pro323Ala
NM_001164783.2:c.964C>G	NP_001158255.1:p.Pro322Ala