Canonical Allele Identifier: CA2336459337
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422910C= , CM000681.2:g.41422910C= GRCh38
NC_000019.9:g.41928815C= , CM000681.1:g.41928815C= GRCh37
NC_000019.8:g.46620655C= NCBI36
NG_013004.1:g.30122C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.996-88C= MANE Select ENSP00000269980.2:n.996-88C=
ENST00000269980.6:c.996-88C= ENSP00000269980.2:n.996-88C=
ENST00000457836.6:c.930-13C= ENSP00000416000.2:n.930-13C=
ENST00000540732.3:c.1098-88C= ENSP00000443246.1:n.1098-88C=
ENST00000542943.5:c.909-88C= ENSP00000440345.1:n.909-88C=
ENST00000595085.5:c.922+213C= ENSP00000471150.2:n.922+213C=
NM_000709.3:c.996-88C= NP_000700.1:n.996-88C=
NM_001164783.1:c.993-88C= NP_001158255.1:n.993-88C=
NM_000709.4:c.996-88C= MANE Select NP_000700.1:n.996-88C=
NM_001164783.2:c.993-88C= NP_001158255.1:n.993-88C=