Canonical Allele Identifier: CA2808660239

Gene: ATPAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18018120T>A , CM000679.2:g.18018120T>A	GRCh38
NC_000017.10:g.17921434T>A , CM000679.1:g.17921434T>A	GRCh37
NC_000017.9:g.17862159T>A	NCBI36
NG_012824.1:g.26047A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474627.8:c.*429A>T MANE Select	ENSP00000417190.2:n.*429A>T
ENST00000462733.5:c.*150-1860A>T	ENSP00000463920.1:n.*150-1860A>T
ENST00000474627.7:c.*429A>T	ENSP00000417190.2:n.*429A>T
ENST00000584205.5:c.*33+6504A>T	ENSP00000462899.1:n.*33+6504A>T
ENST00000585101.5:c.*34-1860A>T	ENSP00000463861.1:n.*34-1860A>T
NM_145691.3:c.*429A>T	NP_663729.1:n.*429A>T
XM_011524062.1:c.732+3003A>T	XP_011522364.1:n.732+3003A>T
XM_011524063.1:c.732+3003A>T	XP_011522365.1:n.732+3003A>T
XM_011524064.1:c.432+3003A>T	XP_011522366.1:n.432+3003A>T
XM_011524065.1:c.733-1860A>T	XP_011522367.1:n.733-1860A>T
XM_011524066.1:c.195+3003A>T	XP_011522368.1:n.195+3003A>T
XM_011524065.2:c.733-1860A>T	XP_011522367.1:n.733-1860A>T
XM_017025303.1:c.433-1860A>T	XP_016880792.1:n.433-1860A>T
XR_001752677.2:n.1696A>T
NM_145691.4:c.*429A>T MANE Select	NP_663729.1:n.*429A>T