Canonical Allele Identifier: CA406005641

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41916865T>C (hg19) ; chr19:g.41410960T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41410960T>C , CM000681.2:g.41410960T>C	GRCh38
NC_000019.9:g.41916865T>C , CM000681.1:g.41916865T>C	GRCh37
NC_000019.8:g.46608705T>C	NCBI36
NG_013004.1:g.18172T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.326T>C MANE Select	ENSP00000269980.2:p.Met109Thr
ENST00000269980.6:c.326T>C	ENSP00000269980.2:p.Met109Thr
ENST00000457836.6:c.260T>C	ENSP00000416000.2:p.Met87Thr
ENST00000538423.5:n.452T>C
ENST00000540732.3:c.428T>C	ENSP00000443246.1:p.Met143Thr
ENST00000541315.1:c.133T>C
ENST00000542943.5:c.288+144T>C	ENSP00000440345.1:n.288+144T>C
ENST00000595085.5:c.326T>C	ENSP00000471150.2:p.Met109Thr
NM_000709.3:c.326T>C	NP_000700.1:p.Met109Thr
NM_001164783.1:c.326T>C	NP_001158255.1:p.Met109Thr
NM_000709.4:c.326T>C MANE Select	NP_000700.1:p.Met109Thr
NM_001164783.2:c.326T>C	NP_001158255.1:p.Met109Thr