Canonical Allele Identifier: CA2336460082
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424581C= , CM000681.2:g.41424581C= GRCh38
NC_000019.9:g.41930486C= , CM000681.1:g.41930486C= GRCh37
NC_000019.8:g.46622326C= NCBI36
NG_013004.1:g.31793C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1311C= MANE Select ENSP00000269980.2:p.His437=
ENST00000269980.6:c.1311C= ENSP00000269980.2:p.His437=
ENST00000457836.6:c.1320C= ENSP00000416000.2:p.His440=
ENST00000540732.3:c.1413C= ENSP00000443246.1:p.His471=
ENST00000544905.1:c.141C=
ENST00000595085.5:c.922+1884C= ENSP00000471150.2:n.922+1884C=
NM_000709.3:c.1311C= NP_000700.1:p.His437=
NM_001164783.1:c.1308C= NP_001158255.1:p.His436=
NM_000709.4:c.1311C= MANE Select NP_000700.1:p.His437=
NM_001164783.2:c.1308C= NP_001158255.1:p.His436=