Canonical Allele Identifier: CA402354851

Gene: ATP5F1A

Linked Data

• MyVariant Identifiers: chr18:g.43667128A>G (hg19) ; chr18:g.46087162A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46087162A>G , CM000680.2:g.46087162A>G	GRCh38
NC_000018.9:g.43667128A>G , CM000680.1:g.43667128A>G	GRCh37
NC_000018.8:g.41921126A>G	NCBI36
NG_041769.1:g.22072T>C
NG_041769.2:g.27072T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398752.11:c.1022T>C MANE Select	ENSP00000381736.5:p.Val341Ala
ENST00000282050.6:c.1022T>C	ENSP00000282050.2:p.Val341Ala
ENST00000398752.10:c.1022T>C	ENSP00000381736.5:p.Val341Ala
ENST00000586523.1:n.1535T>C
ENST00000586592.5:c.*1085T>C	ENSP00000466275.3:n.*1085T>C
ENST00000590156.5:c.*918T>C	ENSP00000466309.1:n.*918T>C
ENST00000590665.5:c.956T>C	ENSP00000467037.1:p.Val319Ala
ENST00000592364.5:c.227-98T>C	ENSP00000468618.1:n.227-98T>C
ENST00000593152.6:c.872T>C	ENSP00000465477.2:p.Val291Ala
NM_001001935.2:c.872T>C	NP_001001935.1:p.Val291Ala
NM_001001937.1:c.1022T>C	NP_001001937.1:p.Val341Ala
NM_001257334.1:c.956T>C	NP_001244263.1:p.Val319Ala
NM_001257335.1:c.872T>C	NP_001244264.1:p.Val291Ala
NM_004046.5:c.1022T>C	NP_004037.1:p.Val341Ala
XM_011526018.1:c.872T>C	XP_011524320.1:p.Val291Ala
XM_017025789.1:c.1022T>C	XP_016881278.1:p.Val341Ala
NM_004046.6:c.1022T>C MANE Select	NP_004037.1:p.Val341Ala
NM_001001935.3:c.872T>C	NP_001001935.1:p.Val291Ala
NM_001257334.2:c.956T>C	NP_001244263.1:p.Val319Ala
NM_001001937.2:c.1022T>C	NP_001001937.1:p.Val341Ala
NM_001257335.2:c.872T>C	NP_001244264.1:p.Val291Ala