Canonical Allele Identifier: CA2336460096
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424601A= , CM000681.2:g.41424601A= GRCh38
NC_000019.9:g.41930506A= , CM000681.1:g.41930506A= GRCh37
NC_000019.8:g.46622346A= NCBI36
NG_013004.1:g.31813A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1331A= MANE Select ENSP00000269980.2:p.Asp444=
ENST00000269980.6:c.1331A= ENSP00000269980.2:p.Asp444=
ENST00000457836.6:c.1340A= ENSP00000416000.2:p.Asp447=
ENST00000540732.3:c.1433A= ENSP00000443246.1:p.Asp478=
ENST00000544905.1:c.161A=
ENST00000595085.5:c.922+1904A= ENSP00000471150.2:n.922+1904A=
NM_000709.3:c.1331A= NP_000700.1:p.Asp444=
NM_001164783.1:c.1328A= NP_001158255.1:p.Asp443=
NM_000709.4:c.1331A= MANE Select NP_000700.1:p.Asp444=
NM_001164783.2:c.1328A= NP_001158255.1:p.Asp443=