Canonical Allele Identifier: CA503985033

Gene: ATP5F1A

Linked Data

• dbSNP Id: rs919026024
• gnomAD v3: 18-46087443-G-C
• gnomAD v4: 18-46087443-G-C
• MyVariant Identifiers: chr18:g.43667409G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46087443G>C , CM000680.2:g.46087443G>C	GRCh38
NC_000018.9:g.43667409G>C , CM000680.1:g.43667409G>C	GRCh37
NC_000018.8:g.41921407G>C	NCBI36
NG_041769.1:g.21791C>G
NG_041769.2:g.26791C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398752.11:c.849C>G MANE Select	ENSP00000381736.5:p.Ala283=
ENST00000282050.6:c.849C>G	ENSP00000282050.2:p.Ala283=
ENST00000398752.10:c.849C>G	ENSP00000381736.5:p.Ala283=
ENST00000586523.1:n.1254C>G
ENST00000586592.5:c.*912C>G	ENSP00000466275.3:n.*912C>G
ENST00000589252.5:c.582C>G	ENSP00000466975.1:p.Ala194=
ENST00000590156.5:c.*745C>G	ENSP00000466309.1:n.*745C>G
ENST00000590665.5:c.783C>G	ENSP00000467037.1:p.Ala261=
ENST00000592364.5:c.227-379C>G	ENSP00000468618.1:n.227-379C>G
ENST00000593152.6:c.699C>G	ENSP00000465477.2:p.Ala233=
NM_001001935.2:c.699C>G	NP_001001935.1:p.Ala233=
NM_001001937.1:c.849C>G	NP_001001937.1:p.Ala283=
NM_001257334.1:c.783C>G	NP_001244263.1:p.Ala261=
NM_001257335.1:c.699C>G	NP_001244264.1:p.Ala233=
NM_004046.5:c.849C>G	NP_004037.1:p.Ala283=
XM_011526018.1:c.699C>G	XP_011524320.1:p.Ala233=
XM_017025789.1:c.849C>G	XP_016881278.1:p.Ala283=
NM_004046.6:c.849C>G MANE Select	NP_004037.1:p.Ala283=
NM_001001935.3:c.699C>G	NP_001001935.1:p.Ala233=
NM_001257334.2:c.783C>G	NP_001244263.1:p.Ala261=
NM_001001937.2:c.849C>G	NP_001001937.1:p.Ala283=
NM_001257335.2:c.699C>G	NP_001244264.1:p.Ala233=