Canonical Allele Identifier: CA308524460

Gene: BCKDHA

Linked Data

• dbSNP Id: rs924679105
• gnomAD v2: 19-41928261-G-A
• gnomAD v4: 19-41422356-G-A
• MyVariant Identifiers: chr19:g.41928261G>A (hg19) ; chr19:g.41422356G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422356G>A , CM000681.2:g.41422356G>A	GRCh38
NC_000019.9:g.41928261G>A , CM000681.1:g.41928261G>A	GRCh37
NC_000019.8:g.46620101G>A	NCBI36
NG_013004.1:g.29568G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.839G>A MANE Select	ENSP00000269980.2:p.Arg280His
ENST00000269980.6:c.839G>A	ENSP00000269980.2:p.Arg280His
ENST00000457836.6:c.773G>A	ENSP00000416000.2:p.Arg258His
ENST00000535632.5:n.468G>A
ENST00000540732.3:c.941G>A	ENSP00000443246.1:p.Arg314His
ENST00000542943.5:c.752G>A	ENSP00000440345.1:p.Arg251His
ENST00000545787.1:n.467G>A
ENST00000595085.5:c.839G>A	ENSP00000471150.2:p.Arg280His
NM_000709.3:c.839G>A	NP_000700.1:p.Arg280His
NM_001164783.1:c.839G>A	NP_001158255.1:p.Arg280His
NM_000709.4:c.839G>A MANE Select	NP_000700.1:p.Arg280His
NM_001164783.2:c.839G>A	NP_001158255.1:p.Arg280His