Canonical Allele Identifier: CA406015469

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41930436C>A (hg19) ; chr19:g.41424531C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41424531C>A , CM000681.2:g.41424531C>A	GRCh38
NC_000019.9:g.41930436C>A , CM000681.1:g.41930436C>A	GRCh37
NC_000019.8:g.46622276C>A	NCBI36
NG_013004.1:g.31743C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1261C>A MANE Select	ENSP00000269980.2:p.Arg421Ser
ENST00000269980.6:c.1261C>A	ENSP00000269980.2:p.Arg421Ser
ENST00000457836.6:c.1270C>A	ENSP00000416000.2:p.Arg424Ser
ENST00000540732.3:c.1363C>A	ENSP00000443246.1:p.Arg455Ser
ENST00000544905.1:c.91C>A
ENST00000595085.5:c.922+1834C>A	ENSP00000471150.2:n.922+1834C>A
NM_000709.3:c.1261C>A	NP_000700.1:p.Arg421Ser
NM_001164783.1:c.1258C>A	NP_001158255.1:p.Arg420Ser
NM_000709.4:c.1261C>A MANE Select	NP_000700.1:p.Arg421Ser
NM_001164783.2:c.1258C>A	NP_001158255.1:p.Arg420Ser