Canonical Allele Identifier: CA406004757
Gene: BCKDHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41410741C>G , CM000681.2:g.41410741C>G GRCh38
NC_000019.9:g.41916646C>G , CM000681.1:g.41916646C>G GRCh37
NC_000019.8:g.46608486C>G NCBI36
NG_013004.1:g.17953C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.213C>G MANE Select ENSP00000269980.2:p.Asn71Lys
ENST00000269980.6:c.213C>G ENSP00000269980.2:p.Asn71Lys
ENST00000457836.6:c.147C>G ENSP00000416000.2:p.Asn49Lys
ENST00000538423.5:n.233C>G
ENST00000540732.3:c.315C>G ENSP00000443246.1:p.Asn105Lys
ENST00000541315.1:c.20C>G
ENST00000542943.5:c.213C>G ENSP00000440345.1:p.Asn71Lys
ENST00000595085.5:c.213C>G ENSP00000471150.2:p.Asn71Lys
ENST00000604424.1:n.455C>G
NM_000709.3:c.213C>G NP_000700.1:p.Asn71Lys
NM_001164783.1:c.213C>G NP_001158255.1:p.Asn71Lys
NM_000709.4:c.213C>G MANE Select NP_000700.1:p.Asn71Lys
NM_001164783.2:c.213C>G NP_001158255.1:p.Asn71Lys