Canonical Allele Identifier: CA2336459958
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424308A= , CM000681.2:g.41424308A= GRCh38
NC_000019.9:g.41930213A= , CM000681.1:g.41930213A= GRCh37
NC_000019.8:g.46622053A= NCBI36
NG_013004.1:g.31520A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1168-130A= MANE Select ENSP00000269980.2:n.1168-130A=
ENST00000269980.6:c.1168-130A= ENSP00000269980.2:n.1168-130A=
ENST00000457836.6:c.1177-130A= ENSP00000416000.2:n.1177-130A=
ENST00000540732.3:c.1270-130A= ENSP00000443246.1:n.1270-130A=
ENST00000544905.1:c.62-194A=
ENST00000595085.5:c.922+1611A= ENSP00000471150.2:n.922+1611A=
NM_000709.3:c.1168-130A= NP_000700.1:n.1168-130A=
NM_001164783.1:c.1165-130A= NP_001158255.1:n.1165-130A=
NM_000709.4:c.1168-130A= MANE Select NP_000700.1:n.1168-130A=
NM_001164783.2:c.1165-130A= NP_001158255.1:n.1165-130A=