Canonical Allele Identifier: CA2336459289

Gene: BCKDHA

Linked Data

• dbSNP Id: rs1599961774

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422795A>C , CM000681.2:g.41422795A>C	GRCh38
NC_000019.9:g.41928700A>C , CM000681.1:g.41928700A>C	GRCh37
NC_000019.8:g.46620540A>C	NCBI36
NG_013004.1:g.30007A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.995+25A>C MANE Select	ENSP00000269980.2:n.995+25A>C
ENST00000269980.6:c.995+25A>C	ENSP00000269980.2:n.995+25A>C
ENST00000457836.6:c.929+25A>C	ENSP00000416000.2:n.929+25A>C
ENST00000540732.3:c.1097+25A>C	ENSP00000443246.1:n.1097+25A>C
ENST00000542943.5:c.908+25A>C	ENSP00000440345.1:n.908+25A>C
ENST00000595085.5:c.922+98A>C	ENSP00000471150.2:n.922+98A>C
NM_000709.3:c.995+25A>C	NP_000700.1:n.995+25A>C
NM_001164783.1:c.992+25A>C	NP_001158255.1:n.992+25A>C
NM_000709.4:c.995+25A>C MANE Select	NP_000700.1:n.995+25A>C
NM_001164783.2:c.992+25A>C	NP_001158255.1:n.992+25A>C