Canonical Allele Identifier: CA2336460097
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424607G= , CM000681.2:g.41424607G= GRCh38
NC_000019.9:g.41930512G= , CM000681.1:g.41930512G= GRCh37
NC_000019.8:g.46622352G= NCBI36
NG_013004.1:g.31819G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1337G= MANE Select ENSP00000269980.2:p.Ter446=
ENST00000269980.6:c.1337G= ENSP00000269980.2:p.Ter446=
ENST00000457836.6:c.1346G= ENSP00000416000.2:p.Ter449=
ENST00000540732.3:c.1439G= ENSP00000443246.1:p.Ter480=
ENST00000544905.1:c.167G=
ENST00000595085.5:c.922+1910G= ENSP00000471150.2:n.922+1910G=
NM_000709.3:c.1337G= NP_000700.1:p.Ter446=
NM_001164783.1:c.1334G= NP_001158255.1:p.Ter445=
NM_000709.4:c.1337G= MANE Select NP_000700.1:p.Ter446=
NM_001164783.2:c.1334G= NP_001158255.1:p.Ter445=