Canonical Allele Identifier: CA2300669257

Gene: ATP5F1A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46087459G= , CM000680.2:g.46087459G=	GRCh38
NC_000018.9:g.43667425G= , CM000680.1:g.43667425G=	GRCh37
NC_000018.8:g.41921423G=	NCBI36
NG_041769.1:g.21775C=
NG_041769.2:g.26775C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398752.11:c.833C= MANE Select	ENSP00000381736.5:p.Thr278=
ENST00000282050.6:c.833C=	ENSP00000282050.2:p.Thr278=
ENST00000398752.10:c.833C=	ENSP00000381736.5:p.Thr278=
ENST00000586523.1:n.1238C=
ENST00000586592.5:c.*896C=	ENSP00000466275.3:n.*896C=
ENST00000589252.5:c.566C=	ENSP00000466975.1:p.Thr189=
ENST00000590156.5:c.*729C=	ENSP00000466309.1:n.*729C=
ENST00000590665.5:c.767C=	ENSP00000467037.1:p.Thr256=
ENST00000592364.5:c.227-395C=	ENSP00000468618.1:n.227-395C=
ENST00000593152.6:c.683C=	ENSP00000465477.2:p.Thr228=
NM_001001935.2:c.683C=	NP_001001935.1:p.Thr228=
NM_001001937.1:c.833C=	NP_001001937.1:p.Thr278=
NM_001257334.1:c.767C=	NP_001244263.1:p.Thr256=
NM_001257335.1:c.683C=	NP_001244264.1:p.Thr228=
NM_004046.5:c.833C=	NP_004037.1:p.Thr278=
XM_011526018.1:c.683C=	XP_011524320.1:p.Thr228=
XM_017025789.1:c.833C=	XP_016881278.1:p.Thr278=
NM_004046.6:c.833C= MANE Select	NP_004037.1:p.Thr278=
NM_001001935.3:c.683C=	NP_001001935.1:p.Thr228=
NM_001257334.2:c.767C=	NP_001244263.1:p.Thr256=
NM_001001937.2:c.833C=	NP_001001937.1:p.Thr278=
NM_001257335.2:c.683C=	NP_001244264.1:p.Thr228=