Canonical Allele Identifier: CA2336459382
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422981C= , CM000681.2:g.41422981C= GRCh38
NC_000019.9:g.41928886C= , CM000681.1:g.41928886C= GRCh37
NC_000019.8:g.46620726C= NCBI36
NG_013004.1:g.30193C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.996-17C= MANE Select ENSP00000269980.2:n.996-17C=
ENST00000269980.6:c.996-17C= ENSP00000269980.2:n.996-17C=
ENST00000457836.6:c.988C= ENSP00000416000.2:p.Pro330=
ENST00000540732.3:c.1098-17C= ENSP00000443246.1:n.1098-17C=
ENST00000542943.5:c.909-17C= ENSP00000440345.1:n.909-17C=
ENST00000595085.5:c.922+284C= ENSP00000471150.2:n.922+284C=
NM_000709.3:c.996-17C= NP_000700.1:n.996-17C=
NM_001164783.1:c.993-17C= NP_001158255.1:n.993-17C=
NM_000709.4:c.996-17C= MANE Select NP_000700.1:n.996-17C=
NM_001164783.2:c.993-17C= NP_001158255.1:n.993-17C=