Canonical Allele Identifier: CA402355566

Gene: ATP5F1A

Linked Data

• MyVariant Identifiers: chr18:g.43667439A>C (hg19) ; chr18:g.46087473A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398752.11:c.819T>G MANE Select	ENSP00000381736.5:p.Ile273Met
ENST00000282050.6:c.819T>G	ENSP00000282050.2:p.Ile273Met
ENST00000398752.10:c.819T>G	ENSP00000381736.5:p.Ile273Met
ENST00000586523.1:n.1224T>G
ENST00000586592.5:c.*882T>G	ENSP00000466275.3:n.*882T>G
ENST00000589252.5:c.552T>G	ENSP00000466975.1:p.Ile184Met
ENST00000590156.5:c.*715T>G	ENSP00000466309.1:n.*715T>G
ENST00000590665.5:c.753T>G	ENSP00000467037.1:p.Ile251Met
ENST00000592364.5:c.227-409T>G	ENSP00000468618.1:n.227-409T>G
ENST00000593152.6:c.669T>G	ENSP00000465477.2:p.Ile223Met
NM_001001935.2:c.669T>G	NP_001001935.1:p.Ile223Met
NM_001001937.1:c.819T>G	NP_001001937.1:p.Ile273Met
NM_001257334.1:c.753T>G	NP_001244263.1:p.Ile251Met
NM_001257335.1:c.669T>G	NP_001244264.1:p.Ile223Met
NM_004046.5:c.819T>G	NP_004037.1:p.Ile273Met
XM_011526018.1:c.669T>G	XP_011524320.1:p.Ile223Met
XM_017025789.1:c.819T>G	XP_016881278.1:p.Ile273Met
NM_004046.6:c.819T>G MANE Select	NP_004037.1:p.Ile273Met
NM_001001935.3:c.669T>G	NP_001001935.1:p.Ile223Met
NM_001257334.2:c.753T>G	NP_001244263.1:p.Ile251Met
NM_001001937.2:c.819T>G	NP_001001937.1:p.Ile273Met
NM_001257335.2:c.669T>G	NP_001244264.1:p.Ile223Met