Canonical Allele Identifier: CA2250822970

Gene: ATPAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18021272_18021274delinsCAG , CM000679.2:g.18021272_18021274delinsCAG	GRCh38
NC_000017.10:g.17924586_17924588delinsCAG , CM000679.1:g.17924586_17924588delinsCAG	GRCh37
NC_000017.9:g.17865311_17865313delinsCAG	NCBI36
NG_012824.1:g.22893_22895delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474627.8:c.617-36_617-34delinsCTG MANE Select	ENSP00000417190.2:n.617-36_617-34delinsCTG
ENST00000462733.5:c.*34-36_*34-34delinsCTG	ENSP00000463920.1:n.*34-36_*34-34delinsCTG
ENST00000465337.2:n.440_442delinsCTG
ENST00000469327.5:n.527-36_527-34delinsCTG
ENST00000474627.7:c.617-36_617-34delinsCTG	ENSP00000417190.2:n.617-36_617-34delinsCTG
ENST00000488753.1:n.412-36_412-34delinsCTG
ENST00000496852.5:n.1122-36_1122-34delinsCTG
ENST00000581698.1:c.49-2588_49-2586delinsCTG
ENST00000584205.5:c.*33+3350_*33+3352delinsCTG	ENSP00000462899.1:n.*33+3350_*33+3352delinsCTG
ENST00000585101.5:c.*33+3350_*33+3352delinsCTG	ENSP00000463861.1:n.*33+3350_*33+3352delinsCTG
NM_145691.3:c.617-36_617-34delinsCTG	NP_663729.1:n.617-36_617-34delinsCTG
XM_005256848.2:c.617-36_617-34delinsCTG	XP_005256905.1:n.617-36_617-34delinsCTG
XM_011524062.1:c.617-36_617-34delinsCTG	XP_011522364.1:n.617-36_617-34delinsCTG
XM_011524063.1:c.617-36_617-34delinsCTG	XP_011522365.1:n.617-36_617-34delinsCTG
XM_011524064.1:c.317-36_317-34delinsCTG	XP_011522366.1:n.317-36_317-34delinsCTG
XM_011524065.1:c.617-36_617-34delinsCTG	XP_011522367.1:n.617-36_617-34delinsCTG
XM_011524066.1:c.80-36_80-34delinsCTG	XP_011522368.1:n.80-36_80-34delinsCTG
XR_934116.1:n.1015-36_1015-34delinsCTG
XM_005256848.4:c.617-36_617-34delinsCTG	XP_005256905.1:n.617-36_617-34delinsCTG
XM_011524065.2:c.617-36_617-34delinsCTG	XP_011522367.1:n.617-36_617-34delinsCTG
XM_017025302.1:c.317-36_317-34delinsCTG	XP_016880791.1:n.317-36_317-34delinsCTG
XM_017025303.1:c.317-36_317-34delinsCTG	XP_016880792.1:n.317-36_317-34delinsCTG
XR_001752677.2:n.1014-36_1014-34delinsCTG
NM_145691.4:c.617-36_617-34delinsCTG MANE Select	NP_663729.1:n.617-36_617-34delinsCTG