Canonical Allele Identifier: CA2336460069
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424547C= , CM000681.2:g.41424547C= GRCh38
NC_000019.9:g.41930452C= , CM000681.1:g.41930452C= GRCh37
NC_000019.8:g.46622292C= NCBI36
NG_013004.1:g.31759C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1277C= MANE Select ENSP00000269980.2:p.Ser426=
ENST00000269980.6:c.1277C= ENSP00000269980.2:p.Ser426=
ENST00000457836.6:c.1286C= ENSP00000416000.2:p.Ser429=
ENST00000540732.3:c.1379C= ENSP00000443246.1:p.Ser460=
ENST00000544905.1:c.107C=
ENST00000595085.5:c.922+1850C= ENSP00000471150.2:n.922+1850C=
NM_000709.3:c.1277C= NP_000700.1:p.Ser426=
NM_001164783.1:c.1274C= NP_001158255.1:p.Ser425=
NM_000709.4:c.1277C= MANE Select NP_000700.1:p.Ser426=
NM_001164783.2:c.1274C= NP_001158255.1:p.Ser425=