Canonical Allele Identifier: CA2250816889

Gene: ATPAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18018212_18018213delinsAG , CM000679.2:g.18018212_18018213delinsAG	GRCh38
NC_000017.10:g.17921526_17921527delinsAG , CM000679.1:g.17921526_17921527delinsAG	GRCh37
NC_000017.9:g.17862251_17862252delinsAG	NCBI36
NG_012824.1:g.25954_25955delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474627.8:c.*336_*337delinsCT MANE Select	ENSP00000417190.2:n.*336_*337delinsCT
ENST00000462733.5:c.*150-1953_*150-1952delinsCT	ENSP00000463920.1:n.*150-1953_*150-1952delinsCT
ENST00000474627.7:c.*336_*337delinsCT	ENSP00000417190.2:n.*336_*337delinsCT
ENST00000584205.5:c.*33+6411_*33+6412delinsCT	ENSP00000462899.1:n.*33+6411_*33+6412delinsCT
ENST00000585101.5:c.*34-1953_*34-1952delinsCT	ENSP00000463861.1:n.*34-1953_*34-1952delinsCT
NM_145691.3:c.*336_*337delinsCT	NP_663729.1:n.*336_*337delinsCT
XM_011524062.1:c.732+2910_732+2911delinsCT	XP_011522364.1:n.732+2910_732+2911delinsCT
XM_011524063.1:c.732+2910_732+2911delinsCT	XP_011522365.1:n.732+2910_732+2911delinsCT
XM_011524064.1:c.432+2910_432+2911delinsCT	XP_011522366.1:n.432+2910_432+2911delinsCT
XM_011524065.1:c.733-1953_733-1952delinsCT	XP_011522367.1:n.733-1953_733-1952delinsCT
XM_011524066.1:c.195+2910_195+2911delinsCT	XP_011522368.1:n.195+2910_195+2911delinsCT
XM_011524065.2:c.733-1953_733-1952delinsCT	XP_011522367.1:n.733-1953_733-1952delinsCT
XM_017025303.1:c.433-1953_433-1952delinsCT	XP_016880792.1:n.433-1953_433-1952delinsCT
XR_001752677.2:n.1603_1604delinsCT
NM_145691.4:c.*336_*337delinsCT MANE Select	NP_663729.1:n.*336_*337delinsCT