Canonical Allele Identifier: CA2429770724

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53235197_53235198delinsAG , CM000685.2:g.53235197_53235198delinsAG	GRCh38
NC_000023.10:g.53264379_53264380delinsAG , CM000685.1:g.53264379_53264380delinsAG	GRCh37
NC_000023.9:g.53281104_53281105delinsAG	NCBI36
NG_021296.1:g.91143_91144delinsCT
NG_021296.2:g.91153_91154delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3661-14_3661-13delinsCT	ENSP00000516672.1:n.3661-14_3661-13delinsCT
ENST00000638521.1:c.1453+585_1453+586delinsCT
ENST00000638869.1:c.962+585_962+586delinsCT
ENST00000639796.1:c.316+1124_316+1125delinsCT	ENSP00000492252.1:n.316+1124_316+1125delinsCT
ENST00000640005.1:c.514+1124_514+1125delinsCT	ENSP00000491293.1:n.514+1124_514+1125delinsCT
ENST00000640436.1:n.482-14_482-13delinsCT
ENST00000640694.1:c.3452-14_3452-13delinsCT	ENSP00000492403.1:n.3452-14_3452-13delinsCT
ENST00000642864.1:c.3502-14_3502-13delinsCT MANE Select	ENSP00000495726.1:n.3502-14_3502-13delinsCT
ENST00000674510.1:c.3502-14_3502-13delinsCT	ENSP00000502054.1:n.3502-14_3502-13delinsCT
ENST00000675719.1:c.3472-14_3472-13delinsCT	ENSP00000501927.1:n.3472-14_3472-13delinsCT
ENST00000375365.2:c.2837-14_2837-13delinsCT	ENSP00000364514.2:n.2837-14_2837-13delinsCT
ENST00000396435.7:c.3502-14_3502-13delinsCT	ENSP00000379712.3:n.3502-14_3502-13delinsCT
NM_001111125.2:c.3502-14_3502-13delinsCT	NP_001104595.1:n.3502-14_3502-13delinsCT
NM_015075.1:c.2837-14_2837-13delinsCT	NP_055890.1:n.2837-14_2837-13delinsCT
XM_006724579.2:c.3598-14_3598-13delinsCT	XP_006724642.1:n.3598-14_3598-13delinsCT
XM_006724580.2:c.2887-14_2887-13delinsCT	XP_006724643.1:n.2887-14_2887-13delinsCT
XM_006724581.2:c.3597+585_3597+586delinsCT	XP_006724644.1:n.3597+585_3597+586delinsCT
XM_006724582.2:c.3597+585_3597+586delinsCT	XP_006724645.1:n.3597+585_3597+586delinsCT
XM_006724583.2:c.3547+1124_3547+1125delinsCT	XP_006724646.1:n.3547+1124_3547+1125delinsCT
XM_006724584.2:c.3548-14_3548-13delinsCT	XP_006724647.1:n.3548-14_3548-13delinsCT
XM_011530772.1:c.2824-14_2824-13delinsCT	XP_011529074.1:n.2824-14_2824-13delinsCT
XM_011530773.1:c.2791-14_2791-13delinsCT	XP_011529075.1:n.2791-14_2791-13delinsCT
XM_011530775.1:c.3547+1124_3547+1125delinsCT	XP_011529077.1:n.3547+1124_3547+1125delinsCT
XM_006724579.3:c.3598-14_3598-13delinsCT	XP_006724642.1:n.3598-14_3598-13delinsCT
XM_006724580.3:c.2887-14_2887-13delinsCT	XP_006724643.1:n.2887-14_2887-13delinsCT
XM_006724581.4:c.3597+585_3597+586delinsCT	XP_006724644.1:n.3597+585_3597+586delinsCT
XM_006724582.4:c.3597+585_3597+586delinsCT	XP_006724645.1:n.3597+585_3597+586delinsCT
XM_006724583.4:c.3547+1124_3547+1125delinsCT	XP_006724646.1:n.3547+1124_3547+1125delinsCT
XM_006724584.3:c.3548-14_3548-13delinsCT	XP_006724647.1:n.3548-14_3548-13delinsCT
XM_011530773.2:c.2791-14_2791-13delinsCT	XP_011529075.1:n.2791-14_2791-13delinsCT
XM_017029359.2:c.3472-14_3472-13delinsCT	XP_016884848.1:n.3472-14_3472-13delinsCT
XM_017029360.1:c.3004-14_3004-13delinsCT	XP_016884849.1:n.3004-14_3004-13delinsCT
NM_001111125.3:c.3502-14_3502-13delinsCT MANE Select	NP_001104595.1:n.3502-14_3502-13delinsCT
NM_015075.2:c.2837-14_2837-13delinsCT	NP_055890.1:n.2837-14_2837-13delinsCT