Canonical Allele Identifier: CA2336458941
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422098G= , CM000681.2:g.41422098G= GRCh38
NC_000019.9:g.41928003G= , CM000681.1:g.41928003G= GRCh37
NC_000019.8:g.46619843G= NCBI36
NG_013004.1:g.29310G=

Transcript Alleles

HGVS Amino-acid change
ENST00000269980.7:c.647-66G= MANE Select ENSP00000269980.2:n.647-66G=
ENST00000269980.6:c.647-66G= ENSP00000269980.2:n.647-66G=
ENST00000457836.6:c.581-66G= ENSP00000416000.2:n.581-66G=
ENST00000535632.5:n.276-66G=
ENST00000538423.5:n.773-66G=
ENST00000540732.3:c.749-66G= ENSP00000443246.1:n.749-66G=
ENST00000541315.1:c.547-66G=
ENST00000542943.5:c.560-66G= ENSP00000440345.1:n.560-66G=
ENST00000545787.1:n.275-66G=
ENST00000595085.5:c.647-66G= ENSP00000471150.2:n.647-66G=
NM_000709.3:c.647-66G= NP_000700.1:n.647-66G=
NM_001164783.1:c.647-66G= NP_001158255.1:n.647-66G=
NM_000709.4:c.647-66G= MANE Select NP_000700.1:n.647-66G=
NM_001164783.2:c.647-66G= NP_001158255.1:n.647-66G=