Canonical Allele Identifier: CA9461368
Community Standard Title: NM_000709.4(BCKDHA):c.1094G>A (p.Arg365Gln)
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41423096G>A , CM000681.2:g.41423096G>A GRCh38
NC_000019.9:g.41929001G>A , CM000681.1:g.41929001G>A GRCh37
NC_000019.8:g.46620841G>A NCBI36
NG_013004.1:g.30308G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000709.4:c.1094G>A MANE Select NP_000700.1:p.Arg365Gln
ENST00000269980.7:c.1094G>A MANE Select ENSP00000269980.2:p.Arg365Gln
NM_000709.3:c.1094G>A NP_000700.1:p.Arg365Gln
NM_001164783.1:c.1091G>A NP_001158255.1:p.Arg364Gln
NM_001164783.2:c.1091G>A NP_001158255.1:p.Arg364Gln
ENST00000269980.6:c.1094G>A ENSP00000269980.2:p.Arg365Gln
ENST00000457836.6:c.1103G>A ENSP00000416000.2:p.Arg368Gln
ENST00000540732.3:c.1196G>A ENSP00000443246.1:p.Arg399Gln
ENST00000595085.5:c.922+399G>A ENSP00000471150.2:n.922+399G>A