Canonical Allele Identifier: CA402355389

Gene: ATP5F1A

Linked Data

• MyVariant Identifiers: chr18:g.43667398T>C (hg19) ; chr18:g.46087432T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46087432T>C , CM000680.2:g.46087432T>C	GRCh38
NC_000018.9:g.43667398T>C , CM000680.1:g.43667398T>C	GRCh37
NC_000018.8:g.41921396T>C	NCBI36
NG_041769.1:g.21802A>G
NG_041769.2:g.26802A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398752.11:c.860A>G MANE Select	ENSP00000381736.5:p.Tyr287Cys
ENST00000282050.6:c.860A>G	ENSP00000282050.2:p.Tyr287Cys
ENST00000398752.10:c.860A>G	ENSP00000381736.5:p.Tyr287Cys
ENST00000586523.1:n.1265A>G
ENST00000586592.5:c.*923A>G	ENSP00000466275.3:n.*923A>G
ENST00000589252.5:c.593A>G	ENSP00000466975.1:p.Tyr198Cys
ENST00000590156.5:c.*756A>G	ENSP00000466309.1:n.*756A>G
ENST00000590665.5:c.794A>G	ENSP00000467037.1:p.Tyr265Cys
ENST00000592364.5:c.227-368A>G	ENSP00000468618.1:n.227-368A>G
ENST00000593152.6:c.710A>G	ENSP00000465477.2:p.Tyr237Cys
NM_001001935.2:c.710A>G	NP_001001935.1:p.Tyr237Cys
NM_001001937.1:c.860A>G	NP_001001937.1:p.Tyr287Cys
NM_001257334.1:c.794A>G	NP_001244263.1:p.Tyr265Cys
NM_001257335.1:c.710A>G	NP_001244264.1:p.Tyr237Cys
NM_004046.5:c.860A>G	NP_004037.1:p.Tyr287Cys
XM_011526018.1:c.710A>G	XP_011524320.1:p.Tyr237Cys
XM_017025789.1:c.860A>G	XP_016881278.1:p.Tyr287Cys
NM_004046.6:c.860A>G MANE Select	NP_004037.1:p.Tyr287Cys
NM_001001935.3:c.710A>G	NP_001001935.1:p.Tyr237Cys
NM_001257334.2:c.794A>G	NP_001244263.1:p.Tyr265Cys
NM_001001937.2:c.860A>G	NP_001001937.1:p.Tyr287Cys
NM_001257335.2:c.710A>G	NP_001244264.1:p.Tyr237Cys