Canonical Allele Identifier: CA406013220

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928543G>A (hg19) ; chr19:g.41422638G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422638G>A , CM000681.2:g.41422638G>A	GRCh38
NC_000019.9:g.41928543G>A , CM000681.1:g.41928543G>A	GRCh37
NC_000019.8:g.46620383G>A	NCBI36
NG_013004.1:g.29850G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269980.7:c.863G>A MANE Select	ENSP00000269980.2:p.Gly288Asp
ENST00000269980.6:c.863G>A	ENSP00000269980.2:p.Gly288Asp
ENST00000457836.6:c.797G>A	ENSP00000416000.2:p.Gly266Asp
ENST00000535632.5:n.492G>A
ENST00000540732.3:c.965G>A	ENSP00000443246.1:p.Gly322Asp
ENST00000542943.5:c.776G>A	ENSP00000440345.1:p.Gly259Asp
ENST00000545787.1:n.491G>A
ENST00000595085.5:c.863G>A	ENSP00000471150.2:p.Gly288Asp
NM_000709.3:c.863G>A	NP_000700.1:p.Gly288Asp
NM_001164783.1:c.860G>A	NP_001158255.1:p.Gly287Asp
NM_000709.4:c.863G>A MANE Select	NP_000700.1:p.Gly288Asp
NM_001164783.2:c.860G>A	NP_001158255.1:p.Gly287Asp