Canonical Allele Identifier: CA2336459393
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41423001C= , CM000681.2:g.41423001C= GRCh38
NC_000019.9:g.41928906C= , CM000681.1:g.41928906C= GRCh37
NC_000019.8:g.46620746C= NCBI36
NG_013004.1:g.30213C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.999C= MANE Select ENSP00000269980.2:p.Ile333=
ENST00000269980.6:c.999C= ENSP00000269980.2:p.Ile333=
ENST00000457836.6:c.1008C= ENSP00000416000.2:p.Ile336=
ENST00000540732.3:c.1101C= ENSP00000443246.1:p.Ile367=
ENST00000542943.5:c.912C= ENSP00000440345.1:p.Ile304=
ENST00000595085.5:c.922+304C= ENSP00000471150.2:n.922+304C=
NM_000709.3:c.999C= NP_000700.1:p.Ile333=
NM_001164783.1:c.996C= NP_001158255.1:p.Ile332=
NM_000709.4:c.999C= MANE Select NP_000700.1:p.Ile333=
NM_001164783.2:c.996C= NP_001158255.1:p.Ile332=