Canonical Allele Identifier: CA2336459060
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422317A= , CM000681.2:g.41422317A= GRCh38
NC_000019.9:g.41928222A= , CM000681.1:g.41928222A= GRCh37
NC_000019.8:g.46620062A= NCBI36
NG_013004.1:g.29529A=

Transcript Alleles

HGVS Amino-acid change
ENST00000269980.7:c.800A= MANE Select ENSP00000269980.2:p.Asn267=
ENST00000269980.6:c.800A= ENSP00000269980.2:p.Asn267=
ENST00000457836.6:c.734A= ENSP00000416000.2:p.Asn245=
ENST00000535632.5:n.429A=
ENST00000540732.3:c.902A= ENSP00000443246.1:p.Asn301=
ENST00000542943.5:c.713A= ENSP00000440345.1:p.Asn238=
ENST00000545787.1:n.428A=
ENST00000595085.5:c.800A= ENSP00000471150.2:p.Asn267=
NM_000709.3:c.800A= NP_000700.1:p.Asn267=
NM_001164783.1:c.800A= NP_001158255.1:p.Asn267=
NM_000709.4:c.800A= MANE Select NP_000700.1:p.Asn267=
NM_001164783.2:c.800A= NP_001158255.1:p.Asn267=