Canonical Allele Identifier: CA2336458995
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422197A= , CM000681.2:g.41422197A= GRCh38
NC_000019.9:g.41928102A= , CM000681.1:g.41928102A= GRCh37
NC_000019.8:g.46619942A= NCBI36
NG_013004.1:g.29409A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.680A= MANE Select ENSP00000269980.2:p.Asn227=
ENST00000269980.6:c.680A= ENSP00000269980.2:p.Asn227=
ENST00000457836.6:c.614A= ENSP00000416000.2:p.Asn205=
ENST00000535632.5:n.309A=
ENST00000538423.5:n.806A=
ENST00000540732.3:c.782A= ENSP00000443246.1:p.Asn261=
ENST00000541315.1:c.580A=
ENST00000542943.5:c.593A= ENSP00000440345.1:p.Asn198=
ENST00000545787.1:n.308A=
ENST00000595085.5:c.680A= ENSP00000471150.2:p.Asn227=
NM_000709.3:c.680A= NP_000700.1:p.Asn227=
NM_001164783.1:c.680A= NP_001158255.1:p.Asn227=
NM_000709.4:c.680A= MANE Select NP_000700.1:p.Asn227=
NM_001164783.2:c.680A= NP_001158255.1:p.Asn227=