Canonical Allele Identifier: CA402355523
Gene: ATP5F1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46087454A>T , CM000680.2:g.46087454A>T GRCh38
NC_000018.9:g.43667420A>T , CM000680.1:g.43667420A>T GRCh37
NC_000018.8:g.41921418A>T NCBI36
NG_041769.1:g.21780T>A
NG_041769.2:g.26780T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398752.11:c.838T>A MANE Select ENSP00000381736.5:p.Ser280Thr
ENST00000282050.6:c.838T>A ENSP00000282050.2:p.Ser280Thr
ENST00000398752.10:c.838T>A ENSP00000381736.5:p.Ser280Thr
ENST00000586523.1:n.1243T>A
ENST00000586592.5:c.*901T>A ENSP00000466275.3:n.*901T>A
ENST00000589252.5:c.571T>A ENSP00000466975.1:p.Ser191Thr
ENST00000590156.5:c.*734T>A ENSP00000466309.1:n.*734T>A
ENST00000590665.5:c.772T>A ENSP00000467037.1:p.Ser258Thr
ENST00000592364.5:c.227-390T>A ENSP00000468618.1:n.227-390T>A
ENST00000593152.6:c.688T>A ENSP00000465477.2:p.Ser230Thr
NM_001001935.2:c.688T>A NP_001001935.1:p.Ser230Thr
NM_001001937.1:c.838T>A NP_001001937.1:p.Ser280Thr
NM_001257334.1:c.772T>A NP_001244263.1:p.Ser258Thr
NM_001257335.1:c.688T>A NP_001244264.1:p.Ser230Thr
NM_004046.5:c.838T>A NP_004037.1:p.Ser280Thr
XM_011526018.1:c.688T>A XP_011524320.1:p.Ser230Thr
XM_017025789.1:c.838T>A XP_016881278.1:p.Ser280Thr
NM_004046.6:c.838T>A MANE Select NP_004037.1:p.Ser280Thr
NM_001001935.3:c.688T>A NP_001001935.1:p.Ser230Thr
NM_001257334.2:c.772T>A NP_001244263.1:p.Ser258Thr
NM_001001937.2:c.838T>A NP_001001937.1:p.Ser280Thr
NM_001257335.2:c.688T>A NP_001244264.1:p.Ser230Thr