Canonical Allele Identifier: CA2336459404
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41423031A= , CM000681.2:g.41423031A= GRCh38
NC_000019.9:g.41928936A= , CM000681.1:g.41928936A= GRCh37
NC_000019.8:g.46620776A= NCBI36
NG_013004.1:g.30243A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1029A= MANE Select ENSP00000269980.2:p.Ser343=
ENST00000269980.6:c.1029A= ENSP00000269980.2:p.Ser343=
ENST00000457836.6:c.1038A= ENSP00000416000.2:p.Ser346=
ENST00000540732.3:c.1131A= ENSP00000443246.1:p.Ser377=
ENST00000542943.5:c.942A= ENSP00000440345.1:p.Ser314=
ENST00000595085.5:c.922+334A= ENSP00000471150.2:n.922+334A=
NM_000709.3:c.1029A= NP_000700.1:p.Ser343=
NM_001164783.1:c.1026A= NP_001158255.1:p.Ser342=
NM_000709.4:c.1029A= MANE Select NP_000700.1:p.Ser343=
NM_001164783.2:c.1026A= NP_001158255.1:p.Ser342=