Canonical Allele Identifier: CA406012679
Gene: BCKDHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422175G>T , CM000681.2:g.41422175G>T GRCh38
NC_000019.9:g.41928080G>T , CM000681.1:g.41928080G>T GRCh37
NC_000019.8:g.46619920G>T NCBI36
NG_013004.1:g.29387G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.658G>T MANE Select ENSP00000269980.2:p.Ala220Ser
ENST00000269980.6:c.658G>T ENSP00000269980.2:p.Ala220Ser
ENST00000457836.6:c.592G>T ENSP00000416000.2:p.Ala198Ser
ENST00000535632.5:n.287G>T
ENST00000538423.5:n.784G>T
ENST00000540732.3:c.760G>T ENSP00000443246.1:p.Ala254Ser
ENST00000541315.1:c.558G>T
ENST00000542943.5:c.571G>T ENSP00000440345.1:p.Ala191Ser
ENST00000545787.1:n.286G>T
ENST00000595085.5:c.658G>T ENSP00000471150.2:p.Ala220Ser
NM_000709.3:c.658G>T NP_000700.1:p.Ala220Ser
NM_001164783.1:c.658G>T NP_001158255.1:p.Ala220Ser
NM_000709.4:c.658G>T MANE Select NP_000700.1:p.Ala220Ser
NM_001164783.2:c.658G>T NP_001158255.1:p.Ala220Ser