Canonical Allele Identifier: CA406015538

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41930451T>A (hg19) ; chr19:g.41424546T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41424546T>A , CM000681.2:g.41424546T>A	GRCh38
NC_000019.9:g.41930451T>A , CM000681.1:g.41930451T>A	GRCh37
NC_000019.8:g.46622291T>A	NCBI36
NG_013004.1:g.31758T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1276T>A MANE Select	ENSP00000269980.2:p.Ser426Thr
ENST00000269980.6:c.1276T>A	ENSP00000269980.2:p.Ser426Thr
ENST00000457836.6:c.1285T>A	ENSP00000416000.2:p.Ser429Thr
ENST00000540732.3:c.1378T>A	ENSP00000443246.1:p.Ser460Thr
ENST00000544905.1:c.106T>A
ENST00000595085.5:c.922+1849T>A	ENSP00000471150.2:n.922+1849T>A
NM_000709.3:c.1276T>A	NP_000700.1:p.Ser426Thr
NM_001164783.1:c.1273T>A	NP_001158255.1:p.Ser425Thr
NM_000709.4:c.1276T>A MANE Select	NP_000700.1:p.Ser426Thr
NM_001164783.2:c.1273T>A	NP_001158255.1:p.Ser425Thr