Canonical Allele Identifier: CA406013534

Gene: BCKDHA

Linked Data

• dbSNP Id: rs1599961669
• MyVariant Identifiers: chr19:g.41928668A>C (hg19) ; chr19:g.41422763A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422763A>C , CM000681.2:g.41422763A>C	GRCh38
NC_000019.9:g.41928668A>C , CM000681.1:g.41928668A>C	GRCh37
NC_000019.8:g.46620508A>C	NCBI36
NG_013004.1:g.29975A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.988A>C MANE Select	ENSP00000269980.2:p.Thr330Pro
ENST00000269980.6:c.988A>C	ENSP00000269980.2:p.Thr330Pro
ENST00000457836.6:c.922A>C	ENSP00000416000.2:p.Thr308Pro
ENST00000540732.3:c.1090A>C	ENSP00000443246.1:p.Thr364Pro
ENST00000542943.5:c.901A>C	ENSP00000440345.1:p.Thr301Pro
ENST00000595085.5:c.922+66A>C	ENSP00000471150.2:n.922+66A>C
NM_000709.3:c.988A>C	NP_000700.1:p.Thr330Pro
NM_001164783.1:c.985A>C	NP_001158255.1:p.Thr329Pro
NM_000709.4:c.988A>C MANE Select	NP_000700.1:p.Thr330Pro
NM_001164783.2:c.985A>C	NP_001158255.1:p.Thr329Pro