Canonical Allele Identifier: CA9461327

Gene: BCKDHA

Linked Data

• dbSNP Id: rs768141390
• ExAC: 19:41928719 C / T
• gnomAD v2: 19-41928719-C-T
• gnomAD v4: 19-41422814-C-T
• MyVariant Identifiers: chr19:g.41928719C>T (hg19) ; chr19:g.41422814C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422814C>T , CM000681.2:g.41422814C>T	GRCh38
NC_000019.9:g.41928719C>T , CM000681.1:g.41928719C>T	GRCh37
NC_000019.8:g.46620559C>T	NCBI36
NG_013004.1:g.30026C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.995+44C>T MANE Select	ENSP00000269980.2:n.995+44C>T
ENST00000269980.6:c.995+44C>T	ENSP00000269980.2:n.995+44C>T
ENST00000457836.6:c.929+44C>T	ENSP00000416000.2:n.929+44C>T
ENST00000540732.3:c.1097+44C>T	ENSP00000443246.1:n.1097+44C>T
ENST00000542943.5:c.908+44C>T	ENSP00000440345.1:n.908+44C>T
ENST00000595085.5:c.922+117C>T	ENSP00000471150.2:n.922+117C>T
NM_000709.3:c.995+44C>T	NP_000700.1:n.995+44C>T
NM_001164783.1:c.992+44C>T	NP_001158255.1:n.992+44C>T
NM_000709.4:c.995+44C>T MANE Select	NP_000700.1:n.995+44C>T
NM_001164783.2:c.992+44C>T	NP_001158255.1:n.992+44C>T