Canonical Allele Identifier: CA2300669263

Gene: ATP5F1A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46087473A= , CM000680.2:g.46087473A=	GRCh38
NC_000018.9:g.43667439A= , CM000680.1:g.43667439A=	GRCh37
NC_000018.8:g.41921437A=	NCBI36
NG_041769.1:g.21761T=
NG_041769.2:g.26761T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398752.11:c.819T= MANE Select	ENSP00000381736.5:p.Ile273=
ENST00000282050.6:c.819T=	ENSP00000282050.2:p.Ile273=
ENST00000398752.10:c.819T=	ENSP00000381736.5:p.Ile273=
ENST00000586523.1:n.1224T=
ENST00000586592.5:c.*882T=	ENSP00000466275.3:n.*882T=
ENST00000589252.5:c.552T=	ENSP00000466975.1:p.Ile184=
ENST00000590156.5:c.*715T=	ENSP00000466309.1:n.*715T=
ENST00000590665.5:c.753T=	ENSP00000467037.1:p.Ile251=
ENST00000592364.5:c.227-409T=	ENSP00000468618.1:n.227-409T=
ENST00000593152.6:c.669T=	ENSP00000465477.2:p.Ile223=
NM_001001935.2:c.669T=	NP_001001935.1:p.Ile223=
NM_001001937.1:c.819T=	NP_001001937.1:p.Ile273=
NM_001257334.1:c.753T=	NP_001244263.1:p.Ile251=
NM_001257335.1:c.669T=	NP_001244264.1:p.Ile223=
NM_004046.5:c.819T=	NP_004037.1:p.Ile273=
XM_011526018.1:c.669T=	XP_011524320.1:p.Ile223=
XM_017025789.1:c.819T=	XP_016881278.1:p.Ile273=
NM_004046.6:c.819T= MANE Select	NP_004037.1:p.Ile273=
NM_001001935.3:c.669T=	NP_001001935.1:p.Ile223=
NM_001257334.2:c.753T=	NP_001244263.1:p.Ile251=
NM_001001937.2:c.819T=	NP_001001937.1:p.Ile273=
NM_001257335.2:c.669T=	NP_001244264.1:p.Ile223=