Canonical Allele Identifier: CA2959535869

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53255803_53255805del , CM000685.2:g.53255803_53255805del	GRCh38
NC_000023.10:g.53284985_53284987del , CM000685.1:g.53284985_53284987del	GRCh37
NC_000023.9:g.53301710_53301712del	NCBI36
NG_021296.1:g.70539_70541del
NG_021296.2:g.70549_70551del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.1156_1158del	ENSP00000516672.1:p.Lys386del
ENST00000638630.1:c.286_288del	ENSP00000492390.1:p.Lys96del
ENST00000640694.1:c.997_999del	ENSP00000492403.1:p.Lys333del
ENST00000642864.1:c.997_999del MANE Select	ENSP00000495726.1:p.Lys333del
ENST00000674510.1:c.997_999del	ENSP00000502054.1:p.Lys333del
ENST00000675719.1:c.967_969del	ENSP00000501927.1:p.Lys323del
ENST00000375365.2:c.382_384del	ENSP00000364514.2:p.Lys128del
ENST00000396435.7:c.997_999del	ENSP00000379712.3:p.Lys333del
NM_001111125.2:c.997_999del	NP_001104595.1:p.Lys333del
NM_015075.1:c.382_384del	NP_055890.1:p.Lys128del
XM_006724579.2:c.1093_1095del	XP_006724642.1:p.Lys365del
XM_006724580.2:c.382_384del	XP_006724643.1:p.Lys128del
XM_006724581.2:c.1093_1095del	XP_006724644.1:p.Lys365del
XM_006724582.2:c.1093_1095del	XP_006724645.1:p.Lys365del
XM_006724583.2:c.1093_1095del	XP_006724646.1:p.Lys365del
XM_006724584.2:c.1093_1095del	XP_006724647.1:p.Lys365del
XM_011530772.1:c.319_321del	XP_011529074.1:p.Lys107del
XM_011530773.1:c.286_288del	XP_011529075.1:p.Lys96del
XM_011530774.1:c.1093_1095del	XP_011529076.1:p.Lys365del
XM_011530775.1:c.1093_1095del	XP_011529077.1:p.Lys365del
XM_011530776.1:c.1093_1095del	XP_011529078.1:p.Lys365del
XM_011530777.1:c.1093_1095del	XP_011529079.1:p.Lys365del
XR_938365.1:n.1320_1322del
XM_006724579.3:c.1093_1095del	XP_006724642.1:p.Lys365del
XM_006724580.3:c.382_384del	XP_006724643.1:p.Lys128del
XM_006724581.4:c.1093_1095del	XP_006724644.1:p.Lys365del
XM_006724582.4:c.1093_1095del	XP_006724645.1:p.Lys365del
XM_006724583.4:c.1093_1095del	XP_006724646.1:p.Lys365del
XM_006724584.3:c.1093_1095del	XP_006724647.1:p.Lys365del
XM_011530773.2:c.286_288del	XP_011529075.1:p.Lys96del
XM_011530774.3:c.1093_1095del	XP_011529076.1:p.Lys365del
XM_011530776.2:c.1093_1095del	XP_011529078.1:p.Lys365del
XM_011530777.2:c.1093_1095del	XP_011529079.1:p.Lys365del
XM_017029359.2:c.967_969del	XP_016884848.1:p.Lys323del
XM_017029360.1:c.499_501del	XP_016884849.1:p.Lys167del
XR_938365.2:n.1314_1316del
NM_001111125.3:c.997_999del MANE Select	NP_001104595.1:p.Lys333del
NM_015075.2:c.382_384del	NP_055890.1:p.Lys128del