Canonical Allele Identifier: CA2576793852

Gene: BCKDHA

Linked Data

• ClinVar Variation Id: 2984610
• ClinVar RCV Id: RCV003845753

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422785C>T , CM000681.2:g.41422785C>T	GRCh38
NC_000019.9:g.41928690C>T , CM000681.1:g.41928690C>T	GRCh37
NC_000019.8:g.46620530C>T	NCBI36
NG_013004.1:g.29997C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.995+15C>T MANE Select	ENSP00000269980.2:n.995+15C>T
ENST00000269980.6:c.995+15C>T	ENSP00000269980.2:n.995+15C>T
ENST00000457836.6:c.929+15C>T	ENSP00000416000.2:n.929+15C>T
ENST00000540732.3:c.1097+15C>T	ENSP00000443246.1:n.1097+15C>T
ENST00000542943.5:c.908+15C>T	ENSP00000440345.1:n.908+15C>T
ENST00000595085.5:c.922+88C>T	ENSP00000471150.2:n.922+88C>T
NM_000709.3:c.995+15C>T	NP_000700.1:n.995+15C>T
NM_001164783.1:c.992+15C>T	NP_001158255.1:n.992+15C>T
NM_000709.4:c.995+15C>T MANE Select	NP_000700.1:n.995+15C>T
NM_001164783.2:c.992+15C>T	NP_001158255.1:n.992+15C>T