Canonical Allele Identifier: CA9461426

Gene: BCKDHA

Linked Data

• dbSNP Id: rs781400345
• ExAC: 19:41930485 A / G
• gnomAD v2: 19-41930485-A-G
• gnomAD v3: 19-41424580-A-G
• gnomAD v4: 19-41424580-A-G
• MyVariant Identifiers: chr19:g.41930485A>G (hg19) ; chr19:g.41424580A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41424580A>G , CM000681.2:g.41424580A>G	GRCh38
NC_000019.9:g.41930485A>G , CM000681.1:g.41930485A>G	GRCh37
NC_000019.8:g.46622325A>G	NCBI36
NG_013004.1:g.31792A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1310A>G MANE Select	ENSP00000269980.2:p.His437Arg
ENST00000269980.6:c.1310A>G	ENSP00000269980.2:p.His437Arg
ENST00000457836.6:c.1319A>G	ENSP00000416000.2:p.His440Arg
ENST00000540732.3:c.1412A>G	ENSP00000443246.1:p.His471Arg
ENST00000544905.1:c.140A>G
ENST00000595085.5:c.922+1883A>G	ENSP00000471150.2:n.922+1883A>G
NM_000709.3:c.1310A>G	NP_000700.1:p.His437Arg
NM_001164783.1:c.1307A>G	NP_001158255.1:p.His436Arg
NM_000709.4:c.1310A>G MANE Select	NP_000700.1:p.His437Arg
NM_001164783.2:c.1307A>G	NP_001158255.1:p.His436Arg