Canonical Allele Identifier: CA2300669224

Gene: ATP5F1A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46087392A= , CM000680.2:g.46087392A=	GRCh38
NC_000018.9:g.43667358A= , CM000680.1:g.43667358A=	GRCh37
NC_000018.8:g.41921356A=	NCBI36
NG_041769.1:g.21842T=
NG_041769.2:g.26842T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398752.11:c.900T= MANE Select	ENSP00000381736.5:p.Phe300=
ENST00000282050.6:c.900T=	ENSP00000282050.2:p.Phe300=
ENST00000398752.10:c.900T=	ENSP00000381736.5:p.Phe300=
ENST00000586523.1:n.1305T=
ENST00000586592.5:c.*963T=	ENSP00000466275.3:n.*963T=
ENST00000590156.5:c.*796T=	ENSP00000466309.1:n.*796T=
ENST00000590665.5:c.834T=	ENSP00000467037.1:p.Phe278=
ENST00000592364.5:c.227-328T=	ENSP00000468618.1:n.227-328T=
ENST00000593152.6:c.750T=	ENSP00000465477.2:p.Phe250=
NM_001001935.2:c.750T=	NP_001001935.1:p.Phe250=
NM_001001937.1:c.900T=	NP_001001937.1:p.Phe300=
NM_001257334.1:c.834T=	NP_001244263.1:p.Phe278=
NM_001257335.1:c.750T=	NP_001244264.1:p.Phe250=
NM_004046.5:c.900T=	NP_004037.1:p.Phe300=
XM_011526018.1:c.750T=	XP_011524320.1:p.Phe250=
XM_017025789.1:c.900T=	XP_016881278.1:p.Phe300=
NM_004046.6:c.900T= MANE Select	NP_004037.1:p.Phe300=
NM_001001935.3:c.750T=	NP_001001935.1:p.Phe250=
NM_001257334.2:c.834T=	NP_001244263.1:p.Phe278=
NM_001001937.2:c.900T=	NP_001001937.1:p.Phe300=
NM_001257335.2:c.750T=	NP_001244264.1:p.Phe250=