Canonical Allele Identifier: CA1139667569

Gene: IQSEC2

Linked Data

• ClinVar Variation Id: 966642
• ClinVar RCV Id: RCV001241371
• dbSNP Id: rs2074374579

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53250764del , CM000685.2:g.53250764del	GRCh38
NC_000023.10:g.53279946del , CM000685.1:g.53279946del	GRCh37
NC_000023.9:g.53296671del	NCBI36
NG_021296.1:g.75578del
NG_021296.2:g.75588del

Transcript Alleles

HGVS	Amino-acid change
ENST00000706952.1:c.1972del	ENSP00000516672.1:p.Asp658ThrfsTer2
ENST00000640694.1:c.1813del	ENSP00000492403.1:p.Asp605ThrfsTer2
ENST00000642864.1:c.1813del MANE Select	ENSP00000495726.1:p.Asp605ThrfsTer2
ENST00000674510.1:c.1813del	ENSP00000502054.1:p.Asp605ThrfsTer2
ENST00000675719.1:c.1783del	ENSP00000501927.1:p.Asp595ThrfsTer2
ENST00000375365.2:c.1198del	ENSP00000364514.2:p.Asp400ThrfsTer2
ENST00000396435.7:c.1813del	ENSP00000379712.3:p.Asp605ThrfsTer2
NM_001111125.2:c.1813del	NP_001104595.1:p.Asp605ThrfsTer2
NM_015075.1:c.1198del	NP_055890.1:p.Asp400ThrfsTer2
XM_006724579.2:c.1909del	XP_006724642.1:p.Asp637ThrfsTer2
XM_006724580.2:c.1198del	XP_006724643.1:p.Asp400ThrfsTer2
XM_006724581.2:c.1909del	XP_006724644.1:p.Asp637ThrfsTer2
XM_006724582.2:c.1909del	XP_006724645.1:p.Asp637ThrfsTer2
XM_006724583.2:c.1909del	XP_006724646.1:p.Asp637ThrfsTer2
XM_006724584.2:c.1909del	XP_006724647.1:p.Asp637ThrfsTer2
XM_011530772.1:c.1135del	XP_011529074.1:p.Asp379ThrfsTer2
XM_011530773.1:c.1102del	XP_011529075.1:p.Asp368ThrfsTer2
XM_011530774.1:c.1909del	XP_011529076.1:p.Asp637ThrfsTer2
XM_011530775.1:c.1909del	XP_011529077.1:p.Asp637ThrfsTer2
XM_011530776.1:c.1909del	XP_011529078.1:p.Asp637ThrfsTer2
XM_011530777.1:c.1909del	XP_011529079.1:p.Asp637ThrfsTer2
XR_938365.1:n.2136del
XM_006724579.3:c.1909del	XP_006724642.1:p.Asp637ThrfsTer2
XM_006724580.3:c.1198del	XP_006724643.1:p.Asp400ThrfsTer2
XM_006724581.4:c.1909del	XP_006724644.1:p.Asp637ThrfsTer2
XM_006724582.4:c.1909del	XP_006724645.1:p.Asp637ThrfsTer2
XM_006724583.4:c.1909del	XP_006724646.1:p.Asp637ThrfsTer2
XM_006724584.3:c.1909del	XP_006724647.1:p.Asp637ThrfsTer2
XM_011530773.2:c.1102del	XP_011529075.1:p.Asp368ThrfsTer2
XM_011530774.3:c.1909del	XP_011529076.1:p.Asp637ThrfsTer2
XM_011530776.2:c.1909del	XP_011529078.1:p.Asp637ThrfsTer2
XM_011530777.2:c.1909del	XP_011529079.1:p.Asp637ThrfsTer2
XM_017029359.2:c.1783del	XP_016884848.1:p.Asp595ThrfsTer2
XM_017029360.1:c.1315del	XP_016884849.1:p.Asp439ThrfsTer2
XR_938365.2:n.2130del
NM_001111125.3:c.1813del MANE Select	NP_001104595.1:p.Asp605ThrfsTer2
NM_015075.2:c.1198del	NP_055890.1:p.Asp400ThrfsTer2