Canonical Allele Identifier: CA398573703
Gene: ATPAF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18021137C>G , CM000679.2:g.18021137C>G GRCh38
NC_000017.10:g.17924451C>G , CM000679.1:g.17924451C>G GRCh37
NC_000017.9:g.17865176C>G NCBI36
NG_012824.1:g.23030G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000474627.8:c.718G>C MANE Select ENSP00000417190.2:p.Glu240Gln
ENST00000462733.5:c.*135G>C ENSP00000463920.1:n.*135G>C
ENST00000465337.2:n.577G>C
ENST00000467560.5:n.128G>C
ENST00000469327.5:n.628G>C
ENST00000474627.7:c.718G>C ENSP00000417190.2:p.Glu240Gln
ENST00000488753.1:n.513G>C
ENST00000496852.5:n.1223G>C
ENST00000581698.1:c.49-2451G>C
ENST00000584205.5:c.*33+3487G>C ENSP00000462899.1:n.*33+3487G>C
ENST00000585101.5:c.*33+3487G>C ENSP00000463861.1:n.*33+3487G>C
NM_145691.3:c.718G>C NP_663729.1:p.Glu240Gln
XM_005256848.2:c.718G>C XP_005256905.1:p.Glu240Gln
XM_011524062.1:c.718G>C XP_011522364.1:p.Glu240Gln
XM_011524063.1:c.718G>C XP_011522365.1:p.Glu240Gln
XM_011524064.1:c.418G>C XP_011522366.1:p.Glu140Gln
XM_011524065.1:c.718G>C XP_011522367.1:p.Glu240Gln
XM_011524066.1:c.181G>C XP_011522368.1:p.Glu61Gln
XM_005256848.4:c.718G>C XP_005256905.1:p.Glu240Gln
XM_011524065.2:c.718G>C XP_011522367.1:p.Glu240Gln
XM_017025302.1:c.418G>C XP_016880791.1:p.Glu140Gln
XM_017025303.1:c.418G>C XP_016880792.1:p.Glu140Gln
XR_001752677.2:n.1115G>C
NM_145691.4:c.718G>C MANE Select NP_663729.1:p.Glu240Gln