Canonical Allele Identifier: CA406012708
Gene: BCKDHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422190C>G , CM000681.2:g.41422190C>G GRCh38
NC_000019.9:g.41928095C>G , CM000681.1:g.41928095C>G GRCh37
NC_000019.8:g.46619935C>G NCBI36
NG_013004.1:g.29402C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000269980.7:c.673C>G MANE Select ENSP00000269980.2:p.Arg225Gly
ENST00000269980.6:c.673C>G ENSP00000269980.2:p.Arg225Gly
ENST00000457836.6:c.607C>G ENSP00000416000.2:p.Arg203Gly
ENST00000535632.5:n.302C>G
ENST00000538423.5:n.799C>G
ENST00000540732.3:c.775C>G ENSP00000443246.1:p.Arg259Gly
ENST00000541315.1:c.573C>G
ENST00000542943.5:c.586C>G ENSP00000440345.1:p.Arg196Gly
ENST00000545787.1:n.301C>G
ENST00000595085.5:c.673C>G ENSP00000471150.2:p.Arg225Gly
NM_000709.3:c.673C>G NP_000700.1:p.Arg225Gly
NM_001164783.1:c.673C>G NP_001158255.1:p.Arg225Gly
NM_000709.4:c.673C>G MANE Select NP_000700.1:p.Arg225Gly
NM_001164783.2:c.673C>G NP_001158255.1:p.Arg225Gly