Canonical Allele Identifier: CA398573667
Gene: ATPAF2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000474627.8:c.722A>T MANE Select ENSP00000417190.2:p.Glu241Val
ENST00000462733.5:c.*139A>T ENSP00000463920.1:n.*139A>T
ENST00000465337.2:n.581A>T
ENST00000467560.5:n.132A>T
ENST00000469327.5:n.632A>T
ENST00000474627.7:c.722A>T ENSP00000417190.2:p.Glu241Val
ENST00000488753.1:n.517A>T
ENST00000496852.5:n.1227A>T
ENST00000581698.1:c.49-2447A>T
ENST00000584205.5:c.*33+3491A>T ENSP00000462899.1:n.*33+3491A>T
ENST00000585101.5:c.*33+3491A>T ENSP00000463861.1:n.*33+3491A>T
NM_145691.3:c.722A>T NP_663729.1:p.Glu241Val
XM_005256848.2:c.722A>T XP_005256905.1:p.Glu241Val
XM_011524062.1:c.722A>T XP_011522364.1:p.Glu241Val
XM_011524063.1:c.722A>T XP_011522365.1:p.Glu241Val
XM_011524064.1:c.422A>T XP_011522366.1:p.Glu141Val
XM_011524065.1:c.722A>T XP_011522367.1:p.Glu241Val
XM_011524066.1:c.185A>T XP_011522368.1:p.Glu62Val
XM_005256848.4:c.722A>T XP_005256905.1:p.Glu241Val
XM_011524065.2:c.722A>T XP_011522367.1:p.Glu241Val
XM_017025302.1:c.422A>T XP_016880791.1:p.Glu141Val
XM_017025303.1:c.422A>T XP_016880792.1:p.Glu141Val
XR_001752677.2:n.1119A>T
NM_145691.4:c.722A>T MANE Select NP_663729.1:p.Glu241Val