Canonical Allele Identifier: CA2820950294

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53235201_53235202insAGAGGTGGAGAAGGAGGAGAAAGAGGAGGAAAAGATGGAGAA , CM000685.2:g.53235201_53235202insAGAGGTGGAGAAGGAGGAGAAAGAGGAGGAAAAGATGGAGAA	GRCh38
NC_000023.10:g.53264383_53264384insAGAGGTGGAGAAGGAGGAGAAAGAGGAGGAAAAGATGGAGAA , CM000685.1:g.53264383_53264384insAGAGGTGGAGAAGGAGGAGAAAGAGGAGGAAAAGATGGAGAA	GRCh37
NC_000023.9:g.53281108_53281109insAGAGGTGGAGAAGGAGGAGAAAGAGGAGGAAAAGATGGAGAA	NCBI36
NG_021296.1:g.91139_91140insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT
NG_021296.2:g.91149_91150insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3661-18_3661-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	ENSP00000516672.1:n.3661-18_3661-17insTTCTCCATCTTTTCCTCCTCTTT...
ENST00000638521.1:c.1453+581_1453+582insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT
ENST00000638869.1:c.962+581_962+582insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT
ENST00000639796.1:c.316+1120_316+1121insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	ENSP00000492252.1:n.316+1120_316+1121insTTCTCCATCTTTTCCTCCTCT...
ENST00000640005.1:c.514+1120_514+1121insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	ENSP00000491293.1:n.514+1120_514+1121insTTCTCCATCTTTTCCTCCTCT...
ENST00000640436.1:n.482-18_482-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT
ENST00000640694.1:c.3452-18_3452-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	ENSP00000492403.1:n.3452-18_3452-17insTTCTCCATCTTTTCCTCCTCTTT...
ENST00000642864.1:c.3502-18_3502-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT MANE Select	ENSP00000495726.1:n.3502-18_3502-17insTTCTCCATCTTTTCCTCCTCTTT...
ENST00000674510.1:c.3502-18_3502-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	ENSP00000502054.1:n.3502-18_3502-17insTTCTCCATCTTTTCCTCCTCTTT...
ENST00000675719.1:c.3472-18_3472-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	ENSP00000501927.1:n.3472-18_3472-17insTTCTCCATCTTTTCCTCCTCTTT...
ENST00000375365.2:c.2837-18_2837-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	ENSP00000364514.2:n.2837-18_2837-17insTTCTCCATCTTTTCCTCCTCTTT...
ENST00000396435.7:c.3502-18_3502-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	ENSP00000379712.3:n.3502-18_3502-17insTTCTCCATCTTTTCCTCCTCTTT...
NM_001111125.2:c.3502-18_3502-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	NP_001104595.1:n.3502-18_3502-17insTTCTCCATCTTTTCCTCCTCTTTCTC...
NM_015075.1:c.2837-18_2837-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	NP_055890.1:n.2837-18_2837-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTC...
XM_006724579.2:c.3598-18_3598-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	XP_006724642.1:n.3598-18_3598-17insTTCTCCATCTTTTCCTCCTCTTTCTC...
XM_006724580.2:c.2887-18_2887-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	XP_006724643.1:n.2887-18_2887-17insTTCTCCATCTTTTCCTCCTCTTTCTC...
XM_006724581.2:c.3597+581_3597+582insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	XP_006724644.1:n.3597+581_3597+582insTTCTCCATCTTTTCCTCCTCTTTC...
XM_006724582.2:c.3597+581_3597+582insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	XP_006724645.1:n.3597+581_3597+582insTTCTCCATCTTTTCCTCCTCTTTC...
XM_006724583.2:c.3547+1120_3547+1121insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	XP_006724646.1:n.3547+1120_3547+1121insTTCTCCATCTTTTCCTCCTCTT...
XM_006724584.2:c.3548-18_3548-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	XP_006724647.1:n.3548-18_3548-17insTTCTCCATCTTTTCCTCCTCTTTCTC...
XM_011530772.1:c.2824-18_2824-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	XP_011529074.1:n.2824-18_2824-17insTTCTCCATCTTTTCCTCCTCTTTCTC...
XM_011530773.1:c.2791-18_2791-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	XP_011529075.1:n.2791-18_2791-17insTTCTCCATCTTTTCCTCCTCTTTCTC...
XM_011530775.1:c.3547+1120_3547+1121insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	XP_011529077.1:n.3547+1120_3547+1121insTTCTCCATCTTTTCCTCCTCTT...
XM_006724579.3:c.3598-18_3598-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	XP_006724642.1:n.3598-18_3598-17insTTCTCCATCTTTTCCTCCTCTTTCTC...
XM_006724580.3:c.2887-18_2887-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	XP_006724643.1:n.2887-18_2887-17insTTCTCCATCTTTTCCTCCTCTTTCTC...
XM_006724581.4:c.3597+581_3597+582insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	XP_006724644.1:n.3597+581_3597+582insTTCTCCATCTTTTCCTCCTCTTTC...
XM_006724582.4:c.3597+581_3597+582insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	XP_006724645.1:n.3597+581_3597+582insTTCTCCATCTTTTCCTCCTCTTTC...
XM_006724583.4:c.3547+1120_3547+1121insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	XP_006724646.1:n.3547+1120_3547+1121insTTCTCCATCTTTTCCTCCTCTT...
XM_006724584.3:c.3548-18_3548-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	XP_006724647.1:n.3548-18_3548-17insTTCTCCATCTTTTCCTCCTCTTTCTC...
XM_011530773.2:c.2791-18_2791-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	XP_011529075.1:n.2791-18_2791-17insTTCTCCATCTTTTCCTCCTCTTTCTC...
XM_017029359.2:c.3472-18_3472-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	XP_016884848.1:n.3472-18_3472-17insTTCTCCATCTTTTCCTCCTCTTTCTC...
XM_017029360.1:c.3004-18_3004-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	XP_016884849.1:n.3004-18_3004-17insTTCTCCATCTTTTCCTCCTCTTTCTC...
NM_001111125.3:c.3502-18_3502-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT MANE Select	NP_001104595.1:n.3502-18_3502-17insTTCTCCATCTTTTCCTCCTCTTTCTC...
NM_015075.2:c.2837-18_2837-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTCCTTCTCCACCTCT	NP_055890.1:n.2837-18_2837-17insTTCTCCATCTTTTCCTCCTCTTTCTCCTC...