Canonical Allele Identifier: CA2250822452
Gene: ATPAF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18021034C= , CM000679.2:g.18021034C= GRCh38
NC_000017.10:g.17924348C= , CM000679.1:g.17924348C= GRCh37
NC_000017.9:g.17865073C= NCBI36
NG_012824.1:g.23133G=

Transcript Alleles

HGVS Amino-acid change
ENST00000474627.8:c.732+89G= MANE Select ENSP00000417190.2:n.732+89G=
ENST00000462733.5:c.*149+89G= ENSP00000463920.1:n.*149+89G=
ENST00000465337.2:n.592-36G=
ENST00000467560.5:n.142+89G=
ENST00000469327.5:n.642+89G=
ENST00000474627.7:c.732+89G= ENSP00000417190.2:n.732+89G=
ENST00000488753.1:n.528-36G=
ENST00000496852.5:n.1237+89G=
ENST00000581698.1:c.49-2348G=
ENST00000584205.5:c.*33+3590G= ENSP00000462899.1:n.*33+3590G=
ENST00000585101.5:c.*33+3590G= ENSP00000463861.1:n.*33+3590G=
NM_145691.3:c.732+89G= NP_663729.1:n.732+89G=
XM_005256848.2:c.733-36G= XP_005256905.1:n.733-36G=
XM_011524062.1:c.732+89G= XP_011522364.1:n.732+89G=
XM_011524063.1:c.732+89G= XP_011522365.1:n.732+89G=
XM_011524064.1:c.432+89G= XP_011522366.1:n.432+89G=
XM_011524065.1:c.732+89G= XP_011522367.1:n.732+89G=
XM_011524066.1:c.195+89G= XP_011522368.1:n.195+89G=
XM_005256848.4:c.733-36G= XP_005256905.1:n.733-36G=
XM_011524065.2:c.732+89G= XP_011522367.1:n.732+89G=
XM_017025302.1:c.432+89G= XP_016880791.1:n.432+89G=
XM_017025303.1:c.432+89G= XP_016880792.1:n.432+89G=
XR_001752677.2:n.1129+89G=
NM_145691.4:c.732+89G= MANE Select NP_663729.1:n.732+89G=