Canonical Allele Identifier: CA2336459183
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422600C= , CM000681.2:g.41422600C= GRCh38
NC_000019.9:g.41928505C= , CM000681.1:g.41928505C= GRCh37
NC_000019.8:g.46620345C= NCBI36
NG_013004.1:g.29812C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.854-29C= MANE Select ENSP00000269980.2:n.854-29C=
ENST00000269980.6:c.854-29C= ENSP00000269980.2:n.854-29C=
ENST00000457836.6:c.788-29C= ENSP00000416000.2:n.788-29C=
ENST00000535632.5:n.483-29C=
ENST00000540732.3:c.956-29C= ENSP00000443246.1:n.956-29C=
ENST00000542943.5:c.767-29C= ENSP00000440345.1:n.767-29C=
ENST00000545787.1:n.482-29C=
ENST00000595085.5:c.854-29C= ENSP00000471150.2:n.854-29C=
NM_000709.3:c.854-29C= NP_000700.1:n.854-29C=
NM_001164783.1:c.854-32C= NP_001158255.1:n.854-32C=
NM_000709.4:c.854-29C= MANE Select NP_000700.1:n.854-29C=
NM_001164783.2:c.854-32C= NP_001158255.1:n.854-32C=