Canonical Allele Identifier: CA2336459362
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422957A= , CM000681.2:g.41422957A= GRCh38
NC_000019.9:g.41928862A= , CM000681.1:g.41928862A= GRCh37
NC_000019.8:g.46620702A= NCBI36
NG_013004.1:g.30169A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.996-41A= MANE Select ENSP00000269980.2:n.996-41A=
ENST00000269980.6:c.996-41A= ENSP00000269980.2:n.996-41A=
ENST00000457836.6:c.964A= ENSP00000416000.2:p.Arg322=
ENST00000540732.3:c.1098-41A= ENSP00000443246.1:n.1098-41A=
ENST00000542943.5:c.909-41A= ENSP00000440345.1:n.909-41A=
ENST00000595085.5:c.922+260A= ENSP00000471150.2:n.922+260A=
NM_000709.3:c.996-41A= NP_000700.1:n.996-41A=
NM_001164783.1:c.993-41A= NP_001158255.1:n.993-41A=
NM_000709.4:c.996-41A= MANE Select NP_000700.1:n.996-41A=
NM_001164783.2:c.993-41A= NP_001158255.1:n.993-41A=