Canonical Allele Identifier: CA503985057
Gene: ATP5F1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.43667418C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46087452C>G , CM000680.2:g.46087452C>G GRCh38
NC_000018.9:g.43667418C>G , CM000680.1:g.43667418C>G GRCh37
NC_000018.8:g.41921416C>G NCBI36
NG_041769.1:g.21782G>C
NG_041769.2:g.26782G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000398752.11:c.840G>C MANE Select ENSP00000381736.5:p.Ser280=
ENST00000282050.6:c.840G>C ENSP00000282050.2:p.Ser280=
ENST00000398752.10:c.840G>C ENSP00000381736.5:p.Ser280=
ENST00000586523.1:n.1245G>C
ENST00000586592.5:c.*903G>C ENSP00000466275.3:n.*903G>C
ENST00000589252.5:c.573G>C ENSP00000466975.1:p.Ser191=
ENST00000590156.5:c.*736G>C ENSP00000466309.1:n.*736G>C
ENST00000590665.5:c.774G>C ENSP00000467037.1:p.Ser258=
ENST00000592364.5:c.227-388G>C ENSP00000468618.1:n.227-388G>C
ENST00000593152.6:c.690G>C ENSP00000465477.2:p.Ser230=
NM_001001935.2:c.690G>C NP_001001935.1:p.Ser230=
NM_001001937.1:c.840G>C NP_001001937.1:p.Ser280=
NM_001257334.1:c.774G>C NP_001244263.1:p.Ser258=
NM_001257335.1:c.690G>C NP_001244264.1:p.Ser230=
NM_004046.5:c.840G>C NP_004037.1:p.Ser280=
XM_011526018.1:c.690G>C XP_011524320.1:p.Ser230=
XM_017025789.1:c.840G>C XP_016881278.1:p.Ser280=
NM_004046.6:c.840G>C MANE Select NP_004037.1:p.Ser280=
NM_001001935.3:c.690G>C NP_001001935.1:p.Ser230=
NM_001257334.2:c.774G>C NP_001244263.1:p.Ser258=
NM_001001937.2:c.840G>C NP_001001937.1:p.Ser280=
NM_001257335.2:c.690G>C NP_001244264.1:p.Ser230=