Canonical Allele Identifier: CA2300669035
Gene: ATP5F1A HGNC NCBI

Linked Data

dbSNP Id: rs1910143148

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.46086935C>A , CM000680.2:g.46086935C>A GRCh38
NC_000018.9:g.43666901C>A , CM000680.1:g.43666901C>A GRCh37
NC_000018.8:g.41920899C>A NCBI36
NG_041769.1:g.22299G>T
NG_041769.2:g.27299G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000398752.11:c.1176+73G>T MANE Select ENSP00000381736.5:n.1176+73G>T
ENST00000282050.6:c.1176+73G>T ENSP00000282050.2:n.1176+73G>T
ENST00000398752.10:c.1176+73G>T ENSP00000381736.5:n.1176+73G>T
ENST00000586523.1:n.1762G>T
ENST00000586592.5:c.*1239+73G>T ENSP00000466275.3:n.*1239+73G>T
ENST00000590156.5:c.*1072+73G>T ENSP00000466309.1:n.*1072+73G>T
ENST00000590665.5:c.1110+73G>T ENSP00000467037.1:n.1110+73G>T
ENST00000592364.5:c.*49+73G>T ENSP00000468618.1:n.*49+73G>T
ENST00000593152.6:c.1026+73G>T ENSP00000465477.2:n.1026+73G>T
NM_001001935.2:c.1026+73G>T NP_001001935.1:n.1026+73G>T
NM_001001937.1:c.1176+73G>T NP_001001937.1:n.1176+73G>T
NM_001257334.1:c.1110+73G>T NP_001244263.1:n.1110+73G>T
NM_001257335.1:c.1026+73G>T NP_001244264.1:n.1026+73G>T
NM_004046.5:c.1176+73G>T NP_004037.1:n.1176+73G>T
XM_011526018.1:c.1026+73G>T XP_011524320.1:n.1026+73G>T
XM_017025789.1:c.1176+73G>T XP_016881278.1:n.1176+73G>T
NM_004046.6:c.1176+73G>T MANE Select NP_004037.1:n.1176+73G>T
NM_001001935.3:c.1026+73G>T NP_001001935.1:n.1026+73G>T
NM_001257334.2:c.1110+73G>T NP_001244263.1:n.1110+73G>T
NM_001001937.2:c.1176+73G>T NP_001001937.1:n.1176+73G>T
NM_001257335.2:c.1026+73G>T NP_001244264.1:n.1026+73G>T