Canonical Allele Identifier: CA9461023

Gene: BCKDHA

Linked Data

• ClinVar Variation Id: 2157258
• ClinVar RCV Id: RCV003078002
• dbSNP Id: rs777414203
• ExAC: 19:41916635 A / G
• gnomAD v2: 19-41916635-A-G
• gnomAD v3: 19-41410730-A-G
• gnomAD v4: 19-41410730-A-G
• MyVariant Identifiers: chr19:g.41916635A>G (hg19) ; chr19:g.41410730A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41410730A>G , CM000681.2:g.41410730A>G	GRCh38
NC_000019.9:g.41916635A>G , CM000681.1:g.41916635A>G	GRCh37
NC_000019.8:g.46608475A>G	NCBI36
NG_013004.1:g.17942A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269980.7:c.202A>G MANE Select	ENSP00000269980.2:p.Ile68Val
ENST00000269980.6:c.202A>G	ENSP00000269980.2:p.Ile68Val
ENST00000457836.6:c.136A>G	ENSP00000416000.2:p.Ile46Val
ENST00000538423.5:n.222A>G
ENST00000540732.3:c.304A>G	ENSP00000443246.1:p.Ile102Val
ENST00000541315.1:c.9A>G
ENST00000542943.5:c.202A>G	ENSP00000440345.1:p.Ile68Val
ENST00000595085.5:c.202A>G	ENSP00000471150.2:p.Ile68Val
ENST00000604424.1:n.444A>G
NM_000709.3:c.202A>G	NP_000700.1:p.Ile68Val
NM_001164783.1:c.202A>G	NP_001158255.1:p.Ile68Val
NM_000709.4:c.202A>G MANE Select	NP_000700.1:p.Ile68Val
NM_001164783.2:c.202A>G	NP_001158255.1:p.Ile68Val