Canonical Allele Identifier: CA9461084
Gene: BCKDHA HGNC NCBI

Linked Data

dbSNP Id: rs749487379

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41410953A>G , CM000681.2:g.41410953A>G GRCh38
NC_000019.9:g.41916858A>G , CM000681.1:g.41916858A>G GRCh37
NC_000019.8:g.46608698A>G NCBI36
NG_013004.1:g.18165A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.319A>G MANE Select ENSP00000269980.2:p.Lys107Glu
ENST00000269980.6:c.319A>G ENSP00000269980.2:p.Lys107Glu
ENST00000457836.6:c.253A>G ENSP00000416000.2:p.Lys85Glu
ENST00000538423.5:n.445A>G
ENST00000540732.3:c.421A>G ENSP00000443246.1:p.Lys141Glu
ENST00000541315.1:c.126A>G
ENST00000542943.5:c.288+137A>G ENSP00000440345.1:n.288+137A>G
ENST00000595085.5:c.319A>G ENSP00000471150.2:p.Lys107Glu
NM_000709.3:c.319A>G NP_000700.1:p.Lys107Glu
NM_001164783.1:c.319A>G NP_001158255.1:p.Lys107Glu
NM_000709.4:c.319A>G MANE Select NP_000700.1:p.Lys107Glu
NM_001164783.2:c.319A>G NP_001158255.1:p.Lys107Glu