Canonical Allele Identifier: CA2429770760

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53235311_53235312delinsAT , CM000685.2:g.53235311_53235312delinsAT	GRCh38
NC_000023.10:g.53264493_53264494delinsAT , CM000685.1:g.53264493_53264494delinsAT	GRCh37
NC_000023.9:g.53281218_53281219delinsAT	NCBI36
NG_021296.1:g.91029_91030delinsAT
NG_021296.2:g.91039_91040delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3661-128_3661-127delinsAT	ENSP00000516672.1:n.3661-128_3661-127delinsAT
ENST00000638521.1:c.1453+471_1453+472delinsAT
ENST00000638869.1:c.962+471_962+472delinsAT
ENST00000639796.1:c.316+1010_316+1011delinsAT	ENSP00000492252.1:n.316+1010_316+1011delinsAT
ENST00000640005.1:c.514+1010_514+1011delinsAT	ENSP00000491293.1:n.514+1010_514+1011delinsAT
ENST00000640436.1:n.482-128_482-127delinsAT
ENST00000640694.1:c.3452-128_3452-127delinsAT	ENSP00000492403.1:n.3452-128_3452-127delinsAT
ENST00000642864.1:c.3502-128_3502-127delinsAT MANE Select	ENSP00000495726.1:n.3502-128_3502-127delinsAT
ENST00000674510.1:c.3502-128_3502-127delinsAT	ENSP00000502054.1:n.3502-128_3502-127delinsAT
ENST00000675719.1:c.3472-128_3472-127delinsAT	ENSP00000501927.1:n.3472-128_3472-127delinsAT
ENST00000375365.2:c.2837-128_2837-127delinsAT	ENSP00000364514.2:n.2837-128_2837-127delinsAT
ENST00000396435.7:c.3502-128_3502-127delinsAT	ENSP00000379712.3:n.3502-128_3502-127delinsAT
NM_001111125.2:c.3502-128_3502-127delinsAT	NP_001104595.1:n.3502-128_3502-127delinsAT
NM_015075.1:c.2837-128_2837-127delinsAT	NP_055890.1:n.2837-128_2837-127delinsAT
XM_006724579.2:c.3598-128_3598-127delinsAT	XP_006724642.1:n.3598-128_3598-127delinsAT
XM_006724580.2:c.2887-128_2887-127delinsAT	XP_006724643.1:n.2887-128_2887-127delinsAT
XM_006724581.2:c.3597+471_3597+472delinsAT	XP_006724644.1:n.3597+471_3597+472delinsAT
XM_006724582.2:c.3597+471_3597+472delinsAT	XP_006724645.1:n.3597+471_3597+472delinsAT
XM_006724583.2:c.3547+1010_3547+1011delinsAT	XP_006724646.1:n.3547+1010_3547+1011delinsAT
XM_006724584.2:c.3548-128_3548-127delinsAT	XP_006724647.1:n.3548-128_3548-127delinsAT
XM_011530772.1:c.2824-128_2824-127delinsAT	XP_011529074.1:n.2824-128_2824-127delinsAT
XM_011530773.1:c.2791-128_2791-127delinsAT	XP_011529075.1:n.2791-128_2791-127delinsAT
XM_011530774.1:c.*175_*176delinsAT	XP_011529076.1:n.*175_*176delinsAT
XM_011530775.1:c.3547+1010_3547+1011delinsAT	XP_011529077.1:n.3547+1010_3547+1011delinsAT
XM_006724579.3:c.3598-128_3598-127delinsAT	XP_006724642.1:n.3598-128_3598-127delinsAT
XM_006724580.3:c.2887-128_2887-127delinsAT	XP_006724643.1:n.2887-128_2887-127delinsAT
XM_006724581.4:c.3597+471_3597+472delinsAT	XP_006724644.1:n.3597+471_3597+472delinsAT
XM_006724582.4:c.3597+471_3597+472delinsAT	XP_006724645.1:n.3597+471_3597+472delinsAT
XM_006724583.4:c.3547+1010_3547+1011delinsAT	XP_006724646.1:n.3547+1010_3547+1011delinsAT
XM_006724584.3:c.3548-128_3548-127delinsAT	XP_006724647.1:n.3548-128_3548-127delinsAT
XM_011530773.2:c.2791-128_2791-127delinsAT	XP_011529075.1:n.2791-128_2791-127delinsAT
XM_011530774.3:c.*175_*176delinsAT	XP_011529076.1:n.*175_*176delinsAT
XM_017029359.2:c.3472-128_3472-127delinsAT	XP_016884848.1:n.3472-128_3472-127delinsAT
XM_017029360.1:c.3004-128_3004-127delinsAT	XP_016884849.1:n.3004-128_3004-127delinsAT
NM_001111125.3:c.3502-128_3502-127delinsAT MANE Select	NP_001104595.1:n.3502-128_3502-127delinsAT
NM_015075.2:c.2837-128_2837-127delinsAT	NP_055890.1:n.2837-128_2837-127delinsAT