Canonical Allele Identifier: CA2250822474
Gene: ATPAF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18021041A= , CM000679.2:g.18021041A= GRCh38
NC_000017.10:g.17924355A= , CM000679.1:g.17924355A= GRCh37
NC_000017.9:g.17865080A= NCBI36
NG_012824.1:g.23126T=

Transcript Alleles

HGVS Amino-acid change
ENST00000474627.8:c.732+82T= MANE Select ENSP00000417190.2:n.732+82T=
ENST00000462733.5:c.*149+82T= ENSP00000463920.1:n.*149+82T=
ENST00000465337.2:n.592-43T=
ENST00000467560.5:n.142+82T=
ENST00000469327.5:n.642+82T=
ENST00000474627.7:c.732+82T= ENSP00000417190.2:n.732+82T=
ENST00000488753.1:n.528-43T=
ENST00000496852.5:n.1237+82T=
ENST00000581698.1:c.49-2355T=
ENST00000584205.5:c.*33+3583T= ENSP00000462899.1:n.*33+3583T=
ENST00000585101.5:c.*33+3583T= ENSP00000463861.1:n.*33+3583T=
NM_145691.3:c.732+82T= NP_663729.1:n.732+82T=
XM_005256848.2:c.733-43T= XP_005256905.1:n.733-43T=
XM_011524062.1:c.732+82T= XP_011522364.1:n.732+82T=
XM_011524063.1:c.732+82T= XP_011522365.1:n.732+82T=
XM_011524064.1:c.432+82T= XP_011522366.1:n.432+82T=
XM_011524065.1:c.732+82T= XP_011522367.1:n.732+82T=
XM_011524066.1:c.195+82T= XP_011522368.1:n.195+82T=
XM_005256848.4:c.733-43T= XP_005256905.1:n.733-43T=
XM_011524065.2:c.732+82T= XP_011522367.1:n.732+82T=
XM_017025302.1:c.432+82T= XP_016880791.1:n.432+82T=
XM_017025303.1:c.432+82T= XP_016880792.1:n.432+82T=
XR_001752677.2:n.1129+82T=
NM_145691.4:c.732+82T= MANE Select NP_663729.1:n.732+82T=