Canonical Allele Identifier: CA2695233924

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53248122_53248136del , CM000685.2:g.53248122_53248136del	GRCh38
NC_000023.10:g.53277304_53277318del , CM000685.1:g.53277304_53277318del	GRCh37
NC_000023.9:g.53294029_53294043del	NCBI36
NG_021296.1:g.78206_78220del
NG_021296.2:g.78216_78230del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.2720_2734del	ENSP00000516672.1:p.Glu907_Glu911del
ENST00000638521.1:c.513_527del
ENST00000638869.1:c.22_36del
ENST00000640694.1:c.2561_2575del	ENSP00000492403.1:p.Glu854_Glu858del
ENST00000642864.1:c.2561_2575del MANE Select	ENSP00000495726.1:p.Glu854_Glu858del
ENST00000674510.1:c.2561_2575del	ENSP00000502054.1:p.Glu854_Glu858del
ENST00000674761.1:n.312_326del
ENST00000675719.1:c.2531_2545del	ENSP00000501927.1:p.Glu844_Glu848del
ENST00000375365.2:c.1946_1960del	ENSP00000364514.2:p.Glu649_Glu653del
ENST00000396435.7:c.2561_2575del	ENSP00000379712.3:p.Glu854_Glu858del
NM_001111125.2:c.2561_2575del	NP_001104595.1:p.Glu854_Glu858del
NM_015075.1:c.1946_1960del	NP_055890.1:p.Glu649_Glu653del
XM_006724579.2:c.2657_2671del	XP_006724642.1:p.Glu886_Glu890del
XM_006724580.2:c.1946_1960del	XP_006724643.1:p.Glu649_Glu653del
XM_006724581.2:c.2657_2671del	XP_006724644.1:p.Glu886_Glu890del
XM_006724582.2:c.2657_2671del	XP_006724645.1:p.Glu886_Glu890del
XM_006724583.2:c.2657_2671del	XP_006724646.1:p.Glu886_Glu890del
XM_006724584.2:c.2657_2671del	XP_006724647.1:p.Glu886_Glu890del
XM_011530772.1:c.1883_1897del	XP_011529074.1:p.Glu628_Glu632del
XM_011530773.1:c.1850_1864del	XP_011529075.1:p.Glu617_Glu621del
XM_011530774.1:c.2657_2671del	XP_011529076.1:p.Glu886_Glu890del
XM_011530775.1:c.2657_2671del	XP_011529077.1:p.Glu886_Glu890del
XM_011530776.1:c.2657_2671del	XP_011529078.1:p.Glu886_Glu890del
XM_011530777.1:c.2657_2671del	XP_011529079.1:p.Glu886_Glu890del
XR_938365.1:n.2884_2898del
XM_006724579.3:c.2657_2671del	XP_006724642.1:p.Glu886_Glu890del
XM_006724580.3:c.1946_1960del	XP_006724643.1:p.Glu649_Glu653del
XM_006724581.4:c.2657_2671del	XP_006724644.1:p.Glu886_Glu890del
XM_006724582.4:c.2657_2671del	XP_006724645.1:p.Glu886_Glu890del
XM_006724583.4:c.2657_2671del	XP_006724646.1:p.Glu886_Glu890del
XM_006724584.3:c.2657_2671del	XP_006724647.1:p.Glu886_Glu890del
XM_011530773.2:c.1850_1864del	XP_011529075.1:p.Glu617_Glu621del
XM_011530774.3:c.2657_2671del	XP_011529076.1:p.Glu886_Glu890del
XM_011530776.2:c.2657_2671del	XP_011529078.1:p.Glu886_Glu890del
XM_011530777.2:c.2657_2671del	XP_011529079.1:p.Glu886_Glu890del
XM_017029359.2:c.2531_2545del	XP_016884848.1:p.Glu844_Glu848del
XM_017029360.1:c.2063_2077del	XP_016884849.1:p.Glu688_Glu692del
XR_938365.2:n.2878_2892del
NM_001111125.3:c.2561_2575del MANE Select	NP_001104595.1:p.Glu854_Glu858del
NM_015075.2:c.1946_1960del	NP_055890.1:p.Glu649_Glu653del