Canonical Allele Identifier: CA406013751

Gene: BCKDHA

Linked Data

• gnomAD v4: 19-41423005-C-T
• MyVariant Identifiers: chr19:g.41928910C>T (hg19) ; chr19:g.41423005C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41423005C>T , CM000681.2:g.41423005C>T	GRCh38
NC_000019.9:g.41928910C>T , CM000681.1:g.41928910C>T	GRCh37
NC_000019.8:g.46620750C>T	NCBI36
NG_013004.1:g.30217C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1003C>T MANE Select	ENSP00000269980.2:p.His335Tyr
ENST00000269980.6:c.1003C>T	ENSP00000269980.2:p.His335Tyr
ENST00000457836.6:c.1012C>T	ENSP00000416000.2:p.His338Tyr
ENST00000540732.3:c.1105C>T	ENSP00000443246.1:p.His369Tyr
ENST00000542943.5:c.916C>T	ENSP00000440345.1:p.His306Tyr
ENST00000595085.5:c.922+308C>T	ENSP00000471150.2:n.922+308C>T
NM_000709.3:c.1003C>T	NP_000700.1:p.His335Tyr
NM_001164783.1:c.1000C>T	NP_001158255.1:p.His334Tyr
NM_000709.4:c.1003C>T MANE Select	NP_000700.1:p.His335Tyr
NM_001164783.2:c.1000C>T	NP_001158255.1:p.His334Tyr