Canonical Allele Identifier: CA406013706
Gene: BCKDHA HGNC NCBI

Linked Data

dbSNP Id: rs201088777

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422987C>A , CM000681.2:g.41422987C>A GRCh38
NC_000019.9:g.41928892C>A , CM000681.1:g.41928892C>A GRCh37
NC_000019.8:g.46620732C>A NCBI36
NG_013004.1:g.30199C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.996-11C>A MANE Select ENSP00000269980.2:n.996-11C>A
ENST00000269980.6:c.996-11C>A ENSP00000269980.2:n.996-11C>A
ENST00000457836.6:c.994C>A ENSP00000416000.2:p.Pro332Thr
ENST00000540732.3:c.1098-11C>A ENSP00000443246.1:n.1098-11C>A
ENST00000542943.5:c.909-11C>A ENSP00000440345.1:n.909-11C>A
ENST00000595085.5:c.922+290C>A ENSP00000471150.2:n.922+290C>A
NM_000709.3:c.996-11C>A NP_000700.1:n.996-11C>A
NM_001164783.1:c.993-11C>A NP_001158255.1:n.993-11C>A
NM_000709.4:c.996-11C>A MANE Select NP_000700.1:n.996-11C>A
NM_001164783.2:c.993-11C>A NP_001158255.1:n.993-11C>A