Canonical Allele Identifier: CA402355452

Gene: ATP5F1A

Linked Data

• MyVariant Identifiers: chr18:g.43667407G>T (hg19) ; chr18:g.46087441G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46087441G>T , CM000680.2:g.46087441G>T	GRCh38
NC_000018.9:g.43667407G>T , CM000680.1:g.43667407G>T	GRCh37
NC_000018.8:g.41921405G>T	NCBI36
NG_041769.1:g.21793C>A
NG_041769.2:g.26793C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398752.11:c.851C>A MANE Select	ENSP00000381736.5:p.Pro284Gln
ENST00000282050.6:c.851C>A	ENSP00000282050.2:p.Pro284Gln
ENST00000398752.10:c.851C>A	ENSP00000381736.5:p.Pro284Gln
ENST00000586523.1:n.1256C>A
ENST00000586592.5:c.*914C>A	ENSP00000466275.3:n.*914C>A
ENST00000589252.5:c.584C>A	ENSP00000466975.1:p.Pro195Gln
ENST00000590156.5:c.*747C>A	ENSP00000466309.1:n.*747C>A
ENST00000590665.5:c.785C>A	ENSP00000467037.1:p.Pro262Gln
ENST00000592364.5:c.227-377C>A	ENSP00000468618.1:n.227-377C>A
ENST00000593152.6:c.701C>A	ENSP00000465477.2:p.Pro234Gln
NM_001001935.2:c.701C>A	NP_001001935.1:p.Pro234Gln
NM_001001937.1:c.851C>A	NP_001001937.1:p.Pro284Gln
NM_001257334.1:c.785C>A	NP_001244263.1:p.Pro262Gln
NM_001257335.1:c.701C>A	NP_001244264.1:p.Pro234Gln
NM_004046.5:c.851C>A	NP_004037.1:p.Pro284Gln
XM_011526018.1:c.701C>A	XP_011524320.1:p.Pro234Gln
XM_017025789.1:c.851C>A	XP_016881278.1:p.Pro284Gln
NM_004046.6:c.851C>A MANE Select	NP_004037.1:p.Pro284Gln
NM_001001935.3:c.701C>A	NP_001001935.1:p.Pro234Gln
NM_001257334.2:c.785C>A	NP_001244263.1:p.Pro262Gln
NM_001001937.2:c.851C>A	NP_001001937.1:p.Pro284Gln
NM_001257335.2:c.701C>A	NP_001244264.1:p.Pro234Gln