Canonical Allele Identifier: CA406013799

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928929A>T (hg19) ; chr19:g.41423024A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41423024A>T , CM000681.2:g.41423024A>T	GRCh38
NC_000019.9:g.41928929A>T , CM000681.1:g.41928929A>T	GRCh37
NC_000019.8:g.46620769A>T	NCBI36
NG_013004.1:g.30236A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1022A>T MANE Select	ENSP00000269980.2:p.Asp341Val
ENST00000269980.6:c.1022A>T	ENSP00000269980.2:p.Asp341Val
ENST00000457836.6:c.1031A>T	ENSP00000416000.2:p.Asp344Val
ENST00000540732.3:c.1124A>T	ENSP00000443246.1:p.Asp375Val
ENST00000542943.5:c.935A>T	ENSP00000440345.1:p.Asp312Val
ENST00000595085.5:c.922+327A>T	ENSP00000471150.2:n.922+327A>T
NM_000709.3:c.1022A>T	NP_000700.1:p.Asp341Val
NM_001164783.1:c.1019A>T	NP_001158255.1:p.Asp340Val
NM_000709.4:c.1022A>T MANE Select	NP_000700.1:p.Asp341Val
NM_001164783.2:c.1019A>T	NP_001158255.1:p.Asp340Val