Canonical Allele Identifier: CA398573665
Gene: ATPAF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18021133T>G , CM000679.2:g.18021133T>G GRCh38
NC_000017.10:g.17924447T>G , CM000679.1:g.17924447T>G GRCh37
NC_000017.9:g.17865172T>G NCBI36
NG_012824.1:g.23034A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000474627.8:c.722A>C MANE Select ENSP00000417190.2:p.Glu241Ala
ENST00000462733.5:c.*139A>C ENSP00000463920.1:n.*139A>C
ENST00000465337.2:n.581A>C
ENST00000467560.5:n.132A>C
ENST00000469327.5:n.632A>C
ENST00000474627.7:c.722A>C ENSP00000417190.2:p.Glu241Ala
ENST00000488753.1:n.517A>C
ENST00000496852.5:n.1227A>C
ENST00000581698.1:c.49-2447A>C
ENST00000584205.5:c.*33+3491A>C ENSP00000462899.1:n.*33+3491A>C
ENST00000585101.5:c.*33+3491A>C ENSP00000463861.1:n.*33+3491A>C
NM_145691.3:c.722A>C NP_663729.1:p.Glu241Ala
XM_005256848.2:c.722A>C XP_005256905.1:p.Glu241Ala
XM_011524062.1:c.722A>C XP_011522364.1:p.Glu241Ala
XM_011524063.1:c.722A>C XP_011522365.1:p.Glu241Ala
XM_011524064.1:c.422A>C XP_011522366.1:p.Glu141Ala
XM_011524065.1:c.722A>C XP_011522367.1:p.Glu241Ala
XM_011524066.1:c.185A>C XP_011522368.1:p.Glu62Ala
XM_005256848.4:c.722A>C XP_005256905.1:p.Glu241Ala
XM_011524065.2:c.722A>C XP_011522367.1:p.Glu241Ala
XM_017025302.1:c.422A>C XP_016880791.1:p.Glu141Ala
XM_017025303.1:c.422A>C XP_016880792.1:p.Glu141Ala
XR_001752677.2:n.1119A>C
NM_145691.4:c.722A>C MANE Select NP_663729.1:p.Glu241Ala