Canonical Allele Identifier: CA406013735

Gene: BCKDHA

Linked Data

• gnomAD v4: 19-41422998-G-T
• MyVariant Identifiers: chr19:g.41928903G>T (hg19) ; chr19:g.41422998G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422998G>T , CM000681.2:g.41422998G>T	GRCh38
NC_000019.9:g.41928903G>T , CM000681.1:g.41928903G>T	GRCh37
NC_000019.8:g.46620743G>T	NCBI36
NG_013004.1:g.30210G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.996G>T MANE Select	ENSP00000269980.2:p.Arg332Ser
ENST00000269980.6:c.996G>T	ENSP00000269980.2:p.Arg332Ser
ENST00000457836.6:c.1005G>T	ENSP00000416000.2:p.Arg335Ser
ENST00000540732.3:c.1098G>T	ENSP00000443246.1:p.Arg366Ser
ENST00000542943.5:c.909G>T	ENSP00000440345.1:p.Arg303Ser
ENST00000595085.5:c.922+301G>T	ENSP00000471150.2:n.922+301G>T
NM_000709.3:c.996G>T	NP_000700.1:p.Arg332Ser
NM_001164783.1:c.993G>T	NP_001158255.1:p.Arg331Ser
NM_000709.4:c.996G>T MANE Select	NP_000700.1:p.Arg332Ser
NM_001164783.2:c.993G>T	NP_001158255.1:p.Arg331Ser