Canonical Allele Identifier: CA2336453929
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41410962A= , CM000681.2:g.41410962A= GRCh38
NC_000019.9:g.41916867A= , CM000681.1:g.41916867A= GRCh37
NC_000019.8:g.46608707A= NCBI36
NG_013004.1:g.18174A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.328A= MANE Select ENSP00000269980.2:p.Thr110=
ENST00000269980.6:c.328A= ENSP00000269980.2:p.Thr110=
ENST00000457836.6:c.262A= ENSP00000416000.2:p.Thr88=
ENST00000538423.5:n.454A=
ENST00000540732.3:c.430A= ENSP00000443246.1:p.Thr144=
ENST00000541315.1:c.135A=
ENST00000542943.5:c.288+146A= ENSP00000440345.1:n.288+146A=
ENST00000595085.5:c.328A= ENSP00000471150.2:p.Thr110=
NM_000709.3:c.328A= NP_000700.1:p.Thr110=
NM_001164783.1:c.328A= NP_001158255.1:p.Thr110=
NM_000709.4:c.328A= MANE Select NP_000700.1:p.Thr110=
NM_001164783.2:c.328A= NP_001158255.1:p.Thr110=