Canonical Allele Identifier: CA2250822966

Gene: ATPAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18021267_18021279delinsCAAAACAGGGCAG , CM000679.2:g.18021267_18021279delinsCAAAACAGGGCAG	GRCh38
NC_000017.10:g.17924581_17924593delinsCAAAACAGGGCAG , CM000679.1:g.17924581_17924593delinsCAAAACAGGGCAG	GRCh37
NC_000017.9:g.17865306_17865318delinsCAAAACAGGGCAG	NCBI36
NG_012824.1:g.22888_22900delinsCTGCCCTGTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474627.8:c.617-41_617-29delinsCTGCCCTGTTTTG MANE Select	ENSP00000417190.2:n.617-41_617-29delinsCTGCCCTGTTTTG
ENST00000462733.5:c.*34-41_*34-29delinsCTGCCCTGTTTTG	ENSP00000463920.1:n.*34-41_*34-29delinsCTGCCCTGTTTTG
ENST00000465337.2:n.435_447delinsCTGCCCTGTTTTG
ENST00000469327.5:n.527-41_527-29delinsCTGCCCTGTTTTG
ENST00000474627.7:c.617-41_617-29delinsCTGCCCTGTTTTG	ENSP00000417190.2:n.617-41_617-29delinsCTGCCCTGTTTTG
ENST00000488753.1:n.412-41_412-29delinsCTGCCCTGTTTTG
ENST00000496852.5:n.1122-41_1122-29delinsCTGCCCTGTTTTG
ENST00000581698.1:c.49-2593_49-2581delinsCTGCCCTGTTTTG
ENST00000584205.5:c.*33+3345_*33+3357delinsCTGCCCTGTTTTG	ENSP00000462899.1:n.*33+3345_*33+3357delinsCTGCCCTGTTTTG
ENST00000585101.5:c.*33+3345_*33+3357delinsCTGCCCTGTTTTG	ENSP00000463861.1:n.*33+3345_*33+3357delinsCTGCCCTGTTTTG
NM_145691.3:c.617-41_617-29delinsCTGCCCTGTTTTG	NP_663729.1:n.617-41_617-29delinsCTGCCCTGTTTTG
XM_005256848.2:c.617-41_617-29delinsCTGCCCTGTTTTG	XP_005256905.1:n.617-41_617-29delinsCTGCCCTGTTTTG
XM_011524062.1:c.617-41_617-29delinsCTGCCCTGTTTTG	XP_011522364.1:n.617-41_617-29delinsCTGCCCTGTTTTG
XM_011524063.1:c.617-41_617-29delinsCTGCCCTGTTTTG	XP_011522365.1:n.617-41_617-29delinsCTGCCCTGTTTTG
XM_011524064.1:c.317-41_317-29delinsCTGCCCTGTTTTG	XP_011522366.1:n.317-41_317-29delinsCTGCCCTGTTTTG
XM_011524065.1:c.617-41_617-29delinsCTGCCCTGTTTTG	XP_011522367.1:n.617-41_617-29delinsCTGCCCTGTTTTG
XM_011524066.1:c.80-41_80-29delinsCTGCCCTGTTTTG	XP_011522368.1:n.80-41_80-29delinsCTGCCCTGTTTTG
XR_934116.1:n.1015-41_1015-29delinsCTGCCCTGTTTTG
XM_005256848.4:c.617-41_617-29delinsCTGCCCTGTTTTG	XP_005256905.1:n.617-41_617-29delinsCTGCCCTGTTTTG
XM_011524065.2:c.617-41_617-29delinsCTGCCCTGTTTTG	XP_011522367.1:n.617-41_617-29delinsCTGCCCTGTTTTG
XM_017025302.1:c.317-41_317-29delinsCTGCCCTGTTTTG	XP_016880791.1:n.317-41_317-29delinsCTGCCCTGTTTTG
XM_017025303.1:c.317-41_317-29delinsCTGCCCTGTTTTG	XP_016880792.1:n.317-41_317-29delinsCTGCCCTGTTTTG
XR_001752677.2:n.1014-41_1014-29delinsCTGCCCTGTTTTG
NM_145691.4:c.617-41_617-29delinsCTGCCCTGTTTTG MANE Select	NP_663729.1:n.617-41_617-29delinsCTGCCCTGTTTTG