Canonical Allele Identifier: CA2336459134
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422471G= , CM000681.2:g.41422471G= GRCh38
NC_000019.9:g.41928376G= , CM000681.1:g.41928376G= GRCh37
NC_000019.8:g.46620216G= NCBI36
NG_013004.1:g.29683G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.853+101G= MANE Select ENSP00000269980.2:n.853+101G=
ENST00000269980.6:c.853+101G= ENSP00000269980.2:n.853+101G=
ENST00000457836.6:c.787+101G= ENSP00000416000.2:n.787+101G=
ENST00000535632.5:n.482+101G=
ENST00000540732.3:c.955+101G= ENSP00000443246.1:n.955+101G=
ENST00000542943.5:c.766+101G= ENSP00000440345.1:n.766+101G=
ENST00000545787.1:n.481+101G=
ENST00000595085.5:c.853+101G= ENSP00000471150.2:n.853+101G=
NM_000709.3:c.853+101G= NP_000700.1:n.853+101G=
NM_001164783.1:c.853+101G= NP_001158255.1:n.853+101G=
NM_000709.4:c.853+101G= MANE Select NP_000700.1:n.853+101G=
NM_001164783.2:c.853+101G= NP_001158255.1:n.853+101G=