Canonical Allele Identifier: CA919978105

Gene: ATP5F1A

Linked Data

• dbSNP Id: rs1599772336

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46087475_46087476insATCAAC , CM000680.2:g.46087475_46087476insATCAAC	GRCh38
NC_000018.9:g.43667441_43667442insATCAAC , CM000680.1:g.43667441_43667442insATCAAC	GRCh37
NC_000018.8:g.41921439_41921440insATCAAC	NCBI36
NG_041769.1:g.21758_21759insGTTGAT
NG_041769.2:g.26758_26759insGTTGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398752.11:c.816_817insGTTGAT MANE Select	ENSP00000381736.5:p.Thr272_Ile273insValAsp
ENST00000282050.6:c.816_817insGTTGAT	ENSP00000282050.2:p.Thr272_Ile273insValAsp
ENST00000398752.10:c.816_817insGTTGAT	ENSP00000381736.5:p.Thr272_Ile273insValAsp
ENST00000586523.1:n.1221_1222insGTTGAT
ENST00000586592.5:c.*879_*880insGTTGAT	ENSP00000466275.3:n.*879_*880insGTTGAT
ENST00000589252.5:c.549_550insGTTGAT	ENSP00000466975.1:p.Thr183_Ile184insValAsp
ENST00000590156.5:c.*712_*713insGTTGAT	ENSP00000466309.1:n.*712_*713insGTTGAT
ENST00000590665.5:c.750_751insGTTGAT	ENSP00000467037.1:p.Thr250_Ile251insValAsp
ENST00000592364.5:c.227-412_227-411insGTTGAT	ENSP00000468618.1:n.227-412_227-411insGTTGAT
ENST00000593152.6:c.666_667insGTTGAT	ENSP00000465477.2:p.Thr222_Ile223insValAsp
NM_001001935.2:c.666_667insGTTGAT	NP_001001935.1:p.Thr222_Ile223insValAsp
NM_001001937.1:c.816_817insGTTGAT	NP_001001937.1:p.Thr272_Ile273insValAsp
NM_001257334.1:c.750_751insGTTGAT	NP_001244263.1:p.Thr250_Ile251insValAsp
NM_001257335.1:c.666_667insGTTGAT	NP_001244264.1:p.Thr222_Ile223insValAsp
NM_004046.5:c.816_817insGTTGAT	NP_004037.1:p.Thr272_Ile273insValAsp
XM_011526018.1:c.666_667insGTTGAT	XP_011524320.1:p.Thr222_Ile223insValAsp
XM_017025789.1:c.816_817insGTTGAT	XP_016881278.1:p.Thr272_Ile273insValAsp
NM_004046.6:c.816_817insGTTGAT MANE Select	NP_004037.1:p.Thr272_Ile273insValAsp
NM_001001935.3:c.666_667insGTTGAT	NP_001001935.1:p.Thr222_Ile223insValAsp
NM_001257334.2:c.750_751insGTTGAT	NP_001244263.1:p.Thr250_Ile251insValAsp
NM_001001937.2:c.816_817insGTTGAT	NP_001001937.1:p.Thr272_Ile273insValAsp
NM_001257335.2:c.666_667insGTTGAT	NP_001244264.1:p.Thr222_Ile223insValAsp