Canonical Allele Identifier: CA402359143
Gene: ATP5F1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46095081A>T , CM000680.2:g.46095081A>T GRCh38
NC_000018.9:g.43675047A>T , CM000680.1:g.43675047A>T GRCh37
NC_000018.8:g.41929045A>T NCBI36
NG_041769.1:g.14153T>A
NG_041769.2:g.19153T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398752.11:c.111T>A MANE Select ENSP00000381736.5:p.His37Gln
ENST00000282050.6:c.111T>A ENSP00000282050.2:p.His37Gln
ENST00000398752.10:c.111T>A ENSP00000381736.5:p.His37Gln
ENST00000585650.1:c.89T>A ENSP00000467983.1:p.Met30Lys
ENST00000586592.5:c.*174T>A ENSP00000466275.3:n.*174T>A
ENST00000588390.1:n.175T>A
ENST00000589252.5:c.111T>A ENSP00000466975.1:p.His37Gln
ENST00000589869.5:c.-40T>A ENSP00000465497.1:n.-40T>A
ENST00000590156.5:c.111T>A ENSP00000466309.1:p.His37Gln
ENST00000590324.5:c.-226T>A ENSP00000465259.1:n.-226T>A
ENST00000590406.5:c.111T>A ENSP00000468458.1:p.His37Gln
ENST00000590448.5:n.168T>A
ENST00000590665.5:c.111T>A ENSP00000467037.1:p.His37Gln
ENST00000591267.1:n.176T>A
ENST00000591981.5:c.127T>A ENSP00000465805.2:p.Cys43Ser
ENST00000592364.5:c.111T>A ENSP00000468618.1:p.His37Gln
ENST00000592989.1:c.-40T>A ENSP00000467830.1:n.-40T>A
ENST00000593152.6:c.-40T>A ENSP00000465477.2:n.-40T>A
NM_001001935.2:c.-113T>A NP_001001935.1:n.-113T>A
NM_001001937.1:c.111T>A NP_001001937.1:p.His37Gln
NM_001257334.1:c.111T>A NP_001244263.1:p.His37Gln
NM_001257335.1:c.-40T>A NP_001244264.1:n.-40T>A
NM_004046.5:c.111T>A NP_004037.1:p.His37Gln
XM_011526018.1:c.-40T>A XP_011524320.1:n.-40T>A
XM_017025789.1:c.111T>A XP_016881278.1:p.His37Gln
NM_004046.6:c.111T>A MANE Select NP_004037.1:p.His37Gln
NM_001001935.3:c.-113T>A NP_001001935.1:n.-113T>A
NM_001257334.2:c.111T>A NP_001244263.1:p.His37Gln
NM_001001937.2:c.111T>A NP_001001937.1:p.His37Gln
NM_001257335.2:c.-40T>A NP_001244264.1:n.-40T>A