Canonical Allele Identifier: CA406015629

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41930476A>C (hg19) ; chr19:g.41424571A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41424571A>C , CM000681.2:g.41424571A>C	GRCh38
NC_000019.9:g.41930476A>C , CM000681.1:g.41930476A>C	GRCh37
NC_000019.8:g.46622316A>C	NCBI36
NG_013004.1:g.31783A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1301A>C MANE Select	ENSP00000269980.2:p.Tyr434Ser
ENST00000269980.6:c.1301A>C	ENSP00000269980.2:p.Tyr434Ser
ENST00000457836.6:c.1310A>C	ENSP00000416000.2:p.Tyr437Ser
ENST00000540732.3:c.1403A>C	ENSP00000443246.1:p.Tyr468Ser
ENST00000544905.1:c.131A>C
ENST00000595085.5:c.922+1874A>C	ENSP00000471150.2:n.922+1874A>C
NM_000709.3:c.1301A>C	NP_000700.1:p.Tyr434Ser
NM_001164783.1:c.1298A>C	NP_001158255.1:p.Tyr433Ser
NM_000709.4:c.1301A>C MANE Select	NP_000700.1:p.Tyr434Ser
NM_001164783.2:c.1298A>C	NP_001158255.1:p.Tyr433Ser