Canonical Allele Identifier: CA2336459073
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422353A= , CM000681.2:g.41422353A= GRCh38
NC_000019.9:g.41928258A= , CM000681.1:g.41928258A= GRCh37
NC_000019.8:g.46620098A= NCBI36
NG_013004.1:g.29565A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.836A= MANE Select ENSP00000269980.2:p.Tyr279=
ENST00000269980.6:c.836A= ENSP00000269980.2:p.Tyr279=
ENST00000457836.6:c.770A= ENSP00000416000.2:p.Tyr257=
ENST00000535632.5:n.465A=
ENST00000540732.3:c.938A= ENSP00000443246.1:p.Tyr313=
ENST00000542943.5:c.749A= ENSP00000440345.1:p.Tyr250=
ENST00000545787.1:n.464A=
ENST00000595085.5:c.836A= ENSP00000471150.2:p.Tyr279=
NM_000709.3:c.836A= NP_000700.1:p.Tyr279=
NM_001164783.1:c.836A= NP_001158255.1:p.Tyr279=
NM_000709.4:c.836A= MANE Select NP_000700.1:p.Tyr279=
NM_001164783.2:c.836A= NP_001158255.1:p.Tyr279=