Canonical Allele Identifier: CA2300669232
Gene: ATP5F1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46087409A= , CM000680.2:g.46087409A= GRCh38
NC_000018.9:g.43667375A= , CM000680.1:g.43667375A= GRCh37
NC_000018.8:g.41921373A= NCBI36
NG_041769.1:g.21825T=
NG_041769.2:g.26825T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000398752.11:c.883T= MANE Select ENSP00000381736.5:p.Ser295=
ENST00000282050.6:c.883T= ENSP00000282050.2:p.Ser295=
ENST00000398752.10:c.883T= ENSP00000381736.5:p.Ser295=
ENST00000586523.1:n.1288T=
ENST00000586592.5:c.*946T= ENSP00000466275.3:n.*946T=
ENST00000590156.5:c.*779T= ENSP00000466309.1:n.*779T=
ENST00000590665.5:c.817T= ENSP00000467037.1:p.Ser273=
ENST00000592364.5:c.227-345T= ENSP00000468618.1:n.227-345T=
ENST00000593152.6:c.733T= ENSP00000465477.2:p.Ser245=
NM_001001935.2:c.733T= NP_001001935.1:p.Ser245=
NM_001001937.1:c.883T= NP_001001937.1:p.Ser295=
NM_001257334.1:c.817T= NP_001244263.1:p.Ser273=
NM_001257335.1:c.733T= NP_001244264.1:p.Ser245=
NM_004046.5:c.883T= NP_004037.1:p.Ser295=
XM_011526018.1:c.733T= XP_011524320.1:p.Ser245=
XM_017025789.1:c.883T= XP_016881278.1:p.Ser295=
NM_004046.6:c.883T= MANE Select NP_004037.1:p.Ser295=
NM_001001935.3:c.733T= NP_001001935.1:p.Ser245=
NM_001257334.2:c.817T= NP_001244263.1:p.Ser273=
NM_001001937.2:c.883T= NP_001001937.1:p.Ser295=
NM_001257335.2:c.733T= NP_001244264.1:p.Ser245=