Canonical Allele Identifier: CA8950679

Gene: ATP5F1A

Linked Data

• dbSNP Id: rs751606511
• ExAC: 18:43667271 C / T
• gnomAD v2: 18-43667271-C-T
• gnomAD v3: 18-46087305-C-T
• gnomAD v4: 18-46087305-C-T
• MyVariant Identifiers: chr18:g.43667271C>T (hg19) ; chr18:g.46087305C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46087305C>T , CM000680.2:g.46087305C>T	GRCh38
NC_000018.9:g.43667271C>T , CM000680.1:g.43667271C>T	GRCh37
NC_000018.8:g.41921269C>T	NCBI36
NG_041769.1:g.21929G>A
NG_041769.2:g.26929G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398752.11:c.951+36G>A MANE Select	ENSP00000381736.5:n.951+36G>A
ENST00000282050.6:c.951+36G>A	ENSP00000282050.2:n.951+36G>A
ENST00000398752.10:c.951+36G>A	ENSP00000381736.5:n.951+36G>A
ENST00000586523.1:n.1392G>A
ENST00000586592.5:c.*1014+36G>A	ENSP00000466275.3:n.*1014+36G>A
ENST00000590156.5:c.*847+36G>A	ENSP00000466309.1:n.*847+36G>A
ENST00000590665.5:c.885+36G>A	ENSP00000467037.1:n.885+36G>A
ENST00000592364.5:c.227-241G>A	ENSP00000468618.1:n.227-241G>A
ENST00000593152.6:c.801+36G>A	ENSP00000465477.2:n.801+36G>A
NM_001001935.2:c.801+36G>A	NP_001001935.1:n.801+36G>A
NM_001001937.1:c.951+36G>A	NP_001001937.1:n.951+36G>A
NM_001257334.1:c.885+36G>A	NP_001244263.1:n.885+36G>A
NM_001257335.1:c.801+36G>A	NP_001244264.1:n.801+36G>A
NM_004046.5:c.951+36G>A	NP_004037.1:n.951+36G>A
XM_011526018.1:c.801+36G>A	XP_011524320.1:n.801+36G>A
XM_017025789.1:c.951+36G>A	XP_016881278.1:n.951+36G>A
NM_004046.6:c.951+36G>A MANE Select	NP_004037.1:n.951+36G>A
NM_001001935.3:c.801+36G>A	NP_001001935.1:n.801+36G>A
NM_001257334.2:c.885+36G>A	NP_001244263.1:n.885+36G>A
NM_001001937.2:c.951+36G>A	NP_001001937.1:n.951+36G>A
NM_001257335.2:c.801+36G>A	NP_001244264.1:n.801+36G>A