Canonical Allele Identifier: CA2250816702

Gene: ATPAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18018054_18018055delinsCA , CM000679.2:g.18018054_18018055delinsCA	GRCh38
NC_000017.10:g.17921368_17921369delinsCA , CM000679.1:g.17921368_17921369delinsCA	GRCh37
NC_000017.9:g.17862093_17862094delinsCA	NCBI36
NG_012824.1:g.26112_26113delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474627.8:c.*494_*495delinsTG MANE Select	ENSP00000417190.2:n.*494_*495delinsTG
ENST00000462733.5:c.*150-1795_*150-1794delinsTG	ENSP00000463920.1:n.*150-1795_*150-1794delinsTG
ENST00000474627.7:c.*494_*495delinsTG	ENSP00000417190.2:n.*494_*495delinsTG
ENST00000584205.5:c.*33+6569_*33+6570delinsTG	ENSP00000462899.1:n.*33+6569_*33+6570delinsTG
ENST00000585101.5:c.*34-1795_*34-1794delinsTG	ENSP00000463861.1:n.*34-1795_*34-1794delinsTG
NM_145691.3:c.*494_*495delinsTG	NP_663729.1:n.*494_*495delinsTG
XM_011524062.1:c.732+3068_732+3069delinsTG	XP_011522364.1:n.732+3068_732+3069delinsTG
XM_011524063.1:c.732+3068_732+3069delinsTG	XP_011522365.1:n.732+3068_732+3069delinsTG
XM_011524064.1:c.432+3068_432+3069delinsTG	XP_011522366.1:n.432+3068_432+3069delinsTG
XM_011524065.1:c.733-1795_733-1794delinsTG	XP_011522367.1:n.733-1795_733-1794delinsTG
XM_011524066.1:c.195+3068_195+3069delinsTG	XP_011522368.1:n.195+3068_195+3069delinsTG
XM_011524065.2:c.733-1795_733-1794delinsTG	XP_011522367.1:n.733-1795_733-1794delinsTG
XM_017025303.1:c.433-1795_433-1794delinsTG	XP_016880792.1:n.433-1795_433-1794delinsTG
XR_001752677.2:n.1761_1762delinsTG
NM_145691.4:c.*494_*495delinsTG MANE Select	NP_663729.1:n.*494_*495delinsTG