Canonical Allele Identifier: CA2336459044
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422282A= , CM000681.2:g.41422282A= GRCh38
NC_000019.9:g.41928187A= , CM000681.1:g.41928187A= GRCh37
NC_000019.8:g.46620027A= NCBI36
NG_013004.1:g.29494A=

Transcript Alleles

HGVS Amino-acid change
ENST00000269980.7:c.765A= MANE Select ENSP00000269980.2:p.Thr255=
ENST00000269980.6:c.765A= ENSP00000269980.2:p.Thr255=
ENST00000457836.6:c.699A= ENSP00000416000.2:p.Thr233=
ENST00000535632.5:n.394A=
ENST00000540732.3:c.867A= ENSP00000443246.1:p.Thr289=
ENST00000542943.5:c.678A= ENSP00000440345.1:p.Thr226=
ENST00000545787.1:n.393A=
ENST00000595085.5:c.765A= ENSP00000471150.2:p.Thr255=
NM_000709.3:c.765A= NP_000700.1:p.Thr255=
NM_001164783.1:c.765A= NP_001158255.1:p.Thr255=
NM_000709.4:c.765A= MANE Select NP_000700.1:p.Thr255=
NM_001164783.2:c.765A= NP_001158255.1:p.Thr255=