Canonical Allele Identifier: CA406013760

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928914A>C (hg19) ; chr19:g.41423009A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41423009A>C , CM000681.2:g.41423009A>C	GRCh38
NC_000019.9:g.41928914A>C , CM000681.1:g.41928914A>C	GRCh37
NC_000019.8:g.46620754A>C	NCBI36
NG_013004.1:g.30221A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1007A>C MANE Select	ENSP00000269980.2:p.His336Pro
ENST00000269980.6:c.1007A>C	ENSP00000269980.2:p.His336Pro
ENST00000457836.6:c.1016A>C	ENSP00000416000.2:p.His339Pro
ENST00000540732.3:c.1109A>C	ENSP00000443246.1:p.His370Pro
ENST00000542943.5:c.920A>C	ENSP00000440345.1:p.His307Pro
ENST00000595085.5:c.922+312A>C	ENSP00000471150.2:n.922+312A>C
NM_000709.3:c.1007A>C	NP_000700.1:p.His336Pro
NM_001164783.1:c.1004A>C	NP_001158255.1:p.His335Pro
NM_000709.4:c.1007A>C MANE Select	NP_000700.1:p.His336Pro
NM_001164783.2:c.1004A>C	NP_001158255.1:p.His335Pro