Canonical Allele Identifier: CA2539960811
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422551T>G , CM000681.2:g.41422551T>G GRCh38
NC_000019.9:g.41928456T>G , CM000681.1:g.41928456T>G GRCh37
NC_000019.8:g.46620296T>G NCBI36
NG_013004.1:g.29763T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.854-78T>G MANE Select ENSP00000269980.2:n.854-78T>G
ENST00000269980.6:c.854-78T>G ENSP00000269980.2:n.854-78T>G
ENST00000457836.6:c.788-78T>G ENSP00000416000.2:n.788-78T>G
ENST00000535632.5:n.483-78T>G
ENST00000540732.3:c.956-78T>G ENSP00000443246.1:n.956-78T>G
ENST00000542943.5:c.767-78T>G ENSP00000440345.1:n.767-78T>G
ENST00000545787.1:n.482-78T>G
ENST00000595085.5:c.854-78T>G ENSP00000471150.2:n.854-78T>G
NM_000709.3:c.854-78T>G NP_000700.1:n.854-78T>G
NM_001164783.1:c.854-81T>G NP_001158255.1:n.854-81T>G
NM_000709.4:c.854-78T>G MANE Select NP_000700.1:n.854-78T>G
NM_001164783.2:c.854-81T>G NP_001158255.1:n.854-81T>G