Canonical Allele Identifier: CA2641640976
Gene: ATP5F1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46087255G>A , CM000680.2:g.46087255G>A GRCh38
NC_000018.9:g.43667221G>A , CM000680.1:g.43667221G>A GRCh37
NC_000018.8:g.41921219G>A NCBI36
NG_041769.1:g.21979C>T
NG_041769.2:g.26979C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000398752.11:c.952-23C>T MANE Select ENSP00000381736.5:n.952-23C>T
ENST00000282050.6:c.952-23C>T ENSP00000282050.2:n.952-23C>T
ENST00000398752.10:c.952-23C>T ENSP00000381736.5:n.952-23C>T
ENST00000586523.1:n.1442C>T
ENST00000586592.5:c.*1015-23C>T ENSP00000466275.3:n.*1015-23C>T
ENST00000590156.5:c.*848-23C>T ENSP00000466309.1:n.*848-23C>T
ENST00000590665.5:c.886-23C>T ENSP00000467037.1:n.886-23C>T
ENST00000592364.5:c.227-191C>T ENSP00000468618.1:n.227-191C>T
ENST00000593152.6:c.802-23C>T ENSP00000465477.2:n.802-23C>T
NM_001001935.2:c.802-23C>T NP_001001935.1:n.802-23C>T
NM_001001937.1:c.952-23C>T NP_001001937.1:n.952-23C>T
NM_001257334.1:c.886-23C>T NP_001244263.1:n.886-23C>T
NM_001257335.1:c.802-23C>T NP_001244264.1:n.802-23C>T
NM_004046.5:c.952-23C>T NP_004037.1:n.952-23C>T
XM_011526018.1:c.802-23C>T XP_011524320.1:n.802-23C>T
XM_017025789.1:c.952-23C>T XP_016881278.1:n.952-23C>T
NM_004046.6:c.952-23C>T MANE Select NP_004037.1:n.952-23C>T
NM_001001935.3:c.802-23C>T NP_001001935.1:n.802-23C>T
NM_001257334.2:c.886-23C>T NP_001244263.1:n.886-23C>T
NM_001001937.2:c.952-23C>T NP_001001937.1:n.952-23C>T
NM_001257335.2:c.802-23C>T NP_001244264.1:n.802-23C>T