Canonical Allele Identifier: CA2250822869

Gene: ATPAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18021223G= , CM000679.2:g.18021223G=	GRCh38
NC_000017.10:g.17924537G= , CM000679.1:g.17924537G=	GRCh37
NC_000017.9:g.17865262G=	NCBI36
NG_012824.1:g.22944C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474627.8:c.632C= MANE Select	ENSP00000417190.2:p.Ala211=
ENST00000462733.5:c.*49C=	ENSP00000463920.1:n.*49C=
ENST00000465337.2:n.491C=
ENST00000467560.5:n.42C=
ENST00000469327.5:n.542C=
ENST00000474627.7:c.632C=	ENSP00000417190.2:p.Ala211=
ENST00000488753.1:n.427C=
ENST00000496852.5:n.1137C=
ENST00000581698.1:c.49-2537C=
ENST00000584205.5:c.*33+3401C=	ENSP00000462899.1:n.*33+3401C=
ENST00000585101.5:c.*33+3401C=	ENSP00000463861.1:n.*33+3401C=
NM_145691.3:c.632C=	NP_663729.1:p.Ala211=
XM_005256848.2:c.632C=	XP_005256905.1:p.Ala211=
XM_011524062.1:c.632C=	XP_011522364.1:p.Ala211=
XM_011524063.1:c.632C=	XP_011522365.1:p.Ala211=
XM_011524064.1:c.332C=	XP_011522366.1:p.Ala111=
XM_011524065.1:c.632C=	XP_011522367.1:p.Ala211=
XM_011524066.1:c.95C=	XP_011522368.1:p.Ala32=
XR_934116.1:n.1030C=
XM_005256848.4:c.632C=	XP_005256905.1:p.Ala211=
XM_011524065.2:c.632C=	XP_011522367.1:p.Ala211=
XM_017025302.1:c.332C=	XP_016880791.1:p.Ala111=
XM_017025303.1:c.332C=	XP_016880792.1:p.Ala111=
XR_001752677.2:n.1029C=
NM_145691.4:c.632C= MANE Select	NP_663729.1:p.Ala211=