Canonical Allele Identifier: CA2336458979
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422170G= , CM000681.2:g.41422170G= GRCh38
NC_000019.9:g.41928075G= , CM000681.1:g.41928075G= GRCh37
NC_000019.8:g.46619915G= NCBI36
NG_013004.1:g.29382G=

Transcript Alleles

HGVS Amino-acid change
ENST00000269980.7:c.653G= MANE Select ENSP00000269980.2:p.Gly218=
ENST00000269980.6:c.653G= ENSP00000269980.2:p.Gly218=
ENST00000457836.6:c.587G= ENSP00000416000.2:p.Gly196=
ENST00000535632.5:n.282G=
ENST00000538423.5:n.779G=
ENST00000540732.3:c.755G= ENSP00000443246.1:p.Gly252=
ENST00000541315.1:c.553G=
ENST00000542943.5:c.566G= ENSP00000440345.1:p.Gly189=
ENST00000545787.1:n.281G=
ENST00000595085.5:c.653G= ENSP00000471150.2:p.Gly218=
NM_000709.3:c.653G= NP_000700.1:p.Gly218=
NM_001164783.1:c.653G= NP_001158255.1:p.Gly218=
NM_000709.4:c.653G= MANE Select NP_000700.1:p.Gly218=
NM_001164783.2:c.653G= NP_001158255.1:p.Gly218=