Canonical Allele Identifier: CA2336459293
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422807C= , CM000681.2:g.41422807C= GRCh38
NC_000019.9:g.41928712C= , CM000681.1:g.41928712C= GRCh37
NC_000019.8:g.46620552C= NCBI36
NG_013004.1:g.30019C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.995+37C= MANE Select ENSP00000269980.2:n.995+37C=
ENST00000269980.6:c.995+37C= ENSP00000269980.2:n.995+37C=
ENST00000457836.6:c.929+37C= ENSP00000416000.2:n.929+37C=
ENST00000540732.3:c.1097+37C= ENSP00000443246.1:n.1097+37C=
ENST00000542943.5:c.908+37C= ENSP00000440345.1:n.908+37C=
ENST00000595085.5:c.922+110C= ENSP00000471150.2:n.922+110C=
NM_000709.3:c.995+37C= NP_000700.1:n.995+37C=
NM_001164783.1:c.992+37C= NP_001158255.1:n.992+37C=
NM_000709.4:c.995+37C= MANE Select NP_000700.1:n.995+37C=
NM_001164783.2:c.992+37C= NP_001158255.1:n.992+37C=