Canonical Allele Identifier: CA406006103
Gene: BCKDHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41411007C>A , CM000681.2:g.41411007C>A GRCh38
NC_000019.9:g.41916912C>A , CM000681.1:g.41916912C>A GRCh37
NC_000019.8:g.46608752C>A NCBI36
NG_013004.1:g.18219C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.373C>A MANE Select ENSP00000269980.2:p.Gln125Lys
ENST00000269980.6:c.373C>A ENSP00000269980.2:p.Gln125Lys
ENST00000457836.6:c.307C>A ENSP00000416000.2:p.Gln103Lys
ENST00000538423.5:n.499C>A
ENST00000540732.3:c.475C>A ENSP00000443246.1:p.Gln159Lys
ENST00000541315.1:c.180C>A
ENST00000542943.5:c.288+191C>A ENSP00000440345.1:n.288+191C>A
ENST00000595085.5:c.373C>A ENSP00000471150.2:p.Gln125Lys
NM_000709.3:c.373C>A NP_000700.1:p.Gln125Lys
NM_001164783.1:c.373C>A NP_001158255.1:p.Gln125Lys
NM_000709.4:c.373C>A MANE Select NP_000700.1:p.Gln125Lys
NM_001164783.2:c.373C>A NP_001158255.1:p.Gln125Lys