Canonical Allele Identifier: CA2300669226

Gene: ATP5F1A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46087397A= , CM000680.2:g.46087397A=	GRCh38
NC_000018.9:g.43667363A= , CM000680.1:g.43667363A=	GRCh37
NC_000018.8:g.41921361A=	NCBI36
NG_041769.1:g.21837T=
NG_041769.2:g.26837T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398752.11:c.895T= MANE Select	ENSP00000381736.5:p.Tyr299=
ENST00000282050.6:c.895T=	ENSP00000282050.2:p.Tyr299=
ENST00000398752.10:c.895T=	ENSP00000381736.5:p.Tyr299=
ENST00000586523.1:n.1300T=
ENST00000586592.5:c.*958T=	ENSP00000466275.3:n.*958T=
ENST00000590156.5:c.*791T=	ENSP00000466309.1:n.*791T=
ENST00000590665.5:c.829T=	ENSP00000467037.1:p.Tyr277=
ENST00000592364.5:c.227-333T=	ENSP00000468618.1:n.227-333T=
ENST00000593152.6:c.745T=	ENSP00000465477.2:p.Tyr249=
NM_001001935.2:c.745T=	NP_001001935.1:p.Tyr249=
NM_001001937.1:c.895T=	NP_001001937.1:p.Tyr299=
NM_001257334.1:c.829T=	NP_001244263.1:p.Tyr277=
NM_001257335.1:c.745T=	NP_001244264.1:p.Tyr249=
NM_004046.5:c.895T=	NP_004037.1:p.Tyr299=
XM_011526018.1:c.745T=	XP_011524320.1:p.Tyr249=
XM_017025789.1:c.895T=	XP_016881278.1:p.Tyr299=
NM_004046.6:c.895T= MANE Select	NP_004037.1:p.Tyr299=
NM_001001935.3:c.745T=	NP_001001935.1:p.Tyr249=
NM_001257334.2:c.829T=	NP_001244263.1:p.Tyr277=
NM_001001937.2:c.895T=	NP_001001937.1:p.Tyr299=
NM_001257335.2:c.745T=	NP_001244264.1:p.Tyr249=