Canonical Allele Identifier: CA402355270

Gene: ATP5F1A

Linked Data

• dbSNP Id: rs77926733
• gnomAD v4: 18-46087406-T-C
• COSMIC: COSM3821487
• MyVariant Identifiers: chr18:g.43667372T>C (hg19) ; chr18:g.46087406T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.46087406T>C , CM000680.2:g.46087406T>C	GRCh38
NC_000018.9:g.43667372T>C , CM000680.1:g.43667372T>C	GRCh37
NC_000018.8:g.41921370T>C	NCBI36
NG_041769.1:g.21828A>G
NG_041769.2:g.26828A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398752.11:c.886A>G MANE Select	ENSP00000381736.5:p.Met296Val
ENST00000282050.6:c.886A>G	ENSP00000282050.2:p.Met296Val
ENST00000398752.10:c.886A>G	ENSP00000381736.5:p.Met296Val
ENST00000586523.1:n.1291A>G
ENST00000586592.5:c.*949A>G	ENSP00000466275.3:n.*949A>G
ENST00000590156.5:c.*782A>G	ENSP00000466309.1:n.*782A>G
ENST00000590665.5:c.820A>G	ENSP00000467037.1:p.Met274Val
ENST00000592364.5:c.227-342A>G	ENSP00000468618.1:n.227-342A>G
ENST00000593152.6:c.736A>G	ENSP00000465477.2:p.Met246Val
NM_001001935.2:c.736A>G	NP_001001935.1:p.Met246Val
NM_001001937.1:c.886A>G	NP_001001937.1:p.Met296Val
NM_001257334.1:c.820A>G	NP_001244263.1:p.Met274Val
NM_001257335.1:c.736A>G	NP_001244264.1:p.Met246Val
NM_004046.5:c.886A>G	NP_004037.1:p.Met296Val
XM_011526018.1:c.736A>G	XP_011524320.1:p.Met246Val
XM_017025789.1:c.886A>G	XP_016881278.1:p.Met296Val
NM_004046.6:c.886A>G MANE Select	NP_004037.1:p.Met296Val
NM_001001935.3:c.736A>G	NP_001001935.1:p.Met246Val
NM_001257334.2:c.820A>G	NP_001244263.1:p.Met274Val
NM_001001937.2:c.886A>G	NP_001001937.1:p.Met296Val
NM_001257335.2:c.736A>G	NP_001244264.1:p.Met246Val