Canonical Allele Identifier: CA2300669261
Gene: ATP5F1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46087465G= , CM000680.2:g.46087465G= GRCh38
NC_000018.9:g.43667431G= , CM000680.1:g.43667431G= GRCh37
NC_000018.8:g.41921429G= NCBI36
NG_041769.1:g.21769C=
NG_041769.2:g.26769C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398752.11:c.827C= MANE Select ENSP00000381736.5:p.Ser276=
ENST00000282050.6:c.827C= ENSP00000282050.2:p.Ser276=
ENST00000398752.10:c.827C= ENSP00000381736.5:p.Ser276=
ENST00000586523.1:n.1232C=
ENST00000586592.5:c.*890C= ENSP00000466275.3:n.*890C=
ENST00000589252.5:c.560C= ENSP00000466975.1:p.Ser187=
ENST00000590156.5:c.*723C= ENSP00000466309.1:n.*723C=
ENST00000590665.5:c.761C= ENSP00000467037.1:p.Ser254=
ENST00000592364.5:c.227-401C= ENSP00000468618.1:n.227-401C=
ENST00000593152.6:c.677C= ENSP00000465477.2:p.Ser226=
NM_001001935.2:c.677C= NP_001001935.1:p.Ser226=
NM_001001937.1:c.827C= NP_001001937.1:p.Ser276=
NM_001257334.1:c.761C= NP_001244263.1:p.Ser254=
NM_001257335.1:c.677C= NP_001244264.1:p.Ser226=
NM_004046.5:c.827C= NP_004037.1:p.Ser276=
XM_011526018.1:c.677C= XP_011524320.1:p.Ser226=
XM_017025789.1:c.827C= XP_016881278.1:p.Ser276=
NM_004046.6:c.827C= MANE Select NP_004037.1:p.Ser276=
NM_001001935.3:c.677C= NP_001001935.1:p.Ser226=
NM_001257334.2:c.761C= NP_001244263.1:p.Ser254=
NM_001001937.2:c.827C= NP_001001937.1:p.Ser276=
NM_001257335.2:c.677C= NP_001244264.1:p.Ser226=