Canonical Allele Identifier: CA2336459151
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422523T= , CM000681.2:g.41422523T= GRCh38
NC_000019.9:g.41928428T= , CM000681.1:g.41928428T= GRCh37
NC_000019.8:g.46620268T= NCBI36
NG_013004.1:g.29735T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.854-106T= MANE Select ENSP00000269980.2:n.854-106T=
ENST00000269980.6:c.854-106T= ENSP00000269980.2:n.854-106T=
ENST00000457836.6:c.788-106T= ENSP00000416000.2:n.788-106T=
ENST00000535632.5:n.483-106T=
ENST00000540732.3:c.956-106T= ENSP00000443246.1:n.956-106T=
ENST00000542943.5:c.767-106T= ENSP00000440345.1:n.767-106T=
ENST00000545787.1:n.482-106T=
ENST00000595085.5:c.854-106T= ENSP00000471150.2:n.854-106T=
NM_000709.3:c.854-106T= NP_000700.1:n.854-106T=
NM_001164783.1:c.854-109T= NP_001158255.1:n.854-109T=
NM_000709.4:c.854-106T= MANE Select NP_000700.1:n.854-106T=
NM_001164783.2:c.854-109T= NP_001158255.1:n.854-109T=