Canonical Allele Identifier: CA2641640740
Gene: ATP5F1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46086775A>C , CM000680.2:g.46086775A>C GRCh38
NC_000018.9:g.43666741A>C , CM000680.1:g.43666741A>C GRCh37
NC_000018.8:g.41920739A>C NCBI36
NG_041769.1:g.22459T>G
NG_041769.2:g.27459T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398752.11:c.1176+233T>G MANE Select ENSP00000381736.5:n.1176+233T>G
ENST00000282050.6:c.1176+233T>G ENSP00000282050.2:n.1176+233T>G
ENST00000398752.10:c.1176+233T>G ENSP00000381736.5:n.1176+233T>G
ENST00000586523.1:n.1922T>G
ENST00000586592.5:c.*1239+233T>G ENSP00000466275.3:n.*1239+233T>G
ENST00000590156.5:c.*1072+233T>G ENSP00000466309.1:n.*1072+233T>G
ENST00000590665.5:c.1110+233T>G ENSP00000467037.1:n.1110+233T>G
ENST00000592364.5:c.*49+233T>G ENSP00000468618.1:n.*49+233T>G
ENST00000593152.6:c.1026+233T>G ENSP00000465477.2:n.1026+233T>G
NM_001001935.2:c.1026+233T>G NP_001001935.1:n.1026+233T>G
NM_001001937.1:c.1176+233T>G NP_001001937.1:n.1176+233T>G
NM_001257334.1:c.1110+233T>G NP_001244263.1:n.1110+233T>G
NM_001257335.1:c.1026+233T>G NP_001244264.1:n.1026+233T>G
NM_004046.5:c.1176+233T>G NP_004037.1:n.1176+233T>G
XM_011526018.1:c.1026+233T>G XP_011524320.1:n.1026+233T>G
XM_017025789.1:c.1176+233T>G XP_016881278.1:n.1176+233T>G
NM_004046.6:c.1176+233T>G MANE Select NP_004037.1:n.1176+233T>G
NM_001001935.3:c.1026+233T>G NP_001001935.1:n.1026+233T>G
NM_001257334.2:c.1110+233T>G NP_001244263.1:n.1110+233T>G
NM_001001937.2:c.1176+233T>G NP_001001937.1:n.1176+233T>G
NM_001257335.2:c.1026+233T>G NP_001244264.1:n.1026+233T>G