Canonical Allele Identifier: CA2336459305
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422835A= , CM000681.2:g.41422835A= GRCh38
NC_000019.9:g.41928740A= , CM000681.1:g.41928740A= GRCh37
NC_000019.8:g.46620580A= NCBI36
NG_013004.1:g.30047A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.995+65A= MANE Select ENSP00000269980.2:n.995+65A=
ENST00000269980.6:c.995+65A= ENSP00000269980.2:n.995+65A=
ENST00000457836.6:c.929+65A= ENSP00000416000.2:n.929+65A=
ENST00000540732.3:c.1097+65A= ENSP00000443246.1:n.1097+65A=
ENST00000542943.5:c.908+65A= ENSP00000440345.1:n.908+65A=
ENST00000595085.5:c.922+138A= ENSP00000471150.2:n.922+138A=
NM_000709.3:c.995+65A= NP_000700.1:n.995+65A=
NM_001164783.1:c.992+65A= NP_001158255.1:n.992+65A=
NM_000709.4:c.995+65A= MANE Select NP_000700.1:n.995+65A=
NM_001164783.2:c.992+65A= NP_001158255.1:n.992+65A=