Canonical Allele Identifier: CA2838609675
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422575T>C , CM000681.2:g.41422575T>C GRCh38
NC_000019.9:g.41928480T>C , CM000681.1:g.41928480T>C GRCh37
NC_000019.8:g.46620320T>C NCBI36
NG_013004.1:g.29787T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.854-54T>C MANE Select ENSP00000269980.2:n.854-54T>C
ENST00000269980.6:c.854-54T>C ENSP00000269980.2:n.854-54T>C
ENST00000457836.6:c.788-54T>C ENSP00000416000.2:n.788-54T>C
ENST00000535632.5:n.483-54T>C
ENST00000540732.3:c.956-54T>C ENSP00000443246.1:n.956-54T>C
ENST00000542943.5:c.767-54T>C ENSP00000440345.1:n.767-54T>C
ENST00000545787.1:n.482-54T>C
ENST00000595085.5:c.854-54T>C ENSP00000471150.2:n.854-54T>C
NM_000709.3:c.854-54T>C NP_000700.1:n.854-54T>C
NM_001164783.1:c.854-57T>C NP_001158255.1:n.854-57T>C
NM_000709.4:c.854-54T>C MANE Select NP_000700.1:n.854-54T>C
NM_001164783.2:c.854-57T>C NP_001158255.1:n.854-57T>C