Canonical Allele Identifier: CA2429772809

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53241815_53241816delinsCG , CM000685.2:g.53241815_53241816delinsCG	GRCh38
NC_000023.10:g.53270997_53270998delinsCG , CM000685.1:g.53270997_53270998delinsCG	GRCh37
NC_000023.9:g.53287722_53287723delinsCG	NCBI36
NG_021296.1:g.84525_84526delinsCG
NG_021296.2:g.84535_84536delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000706952.1:c.3142_3143delinsCG	ENSP00000516672.1:p.Arg1048=
ENST00000638521.1:c.935_936delinsCG
ENST00000638869.1:c.444_445delinsCG
ENST00000639642.1:c.273_274delinsCG
ENST00000640005.1:c.46_47delinsCG	ENSP00000491293.1:p.Arg16=
ENST00000640694.1:c.2983_2984delinsCG	ENSP00000492403.1:p.Arg995=
ENST00000642864.1:c.2983_2984delinsCG MANE Select	ENSP00000495726.1:p.Arg995=
ENST00000674510.1:c.2983_2984delinsCG	ENSP00000502054.1:p.Arg995=
ENST00000674761.1:n.1290_1291delinsCG
ENST00000675719.1:c.2953_2954delinsCG	ENSP00000501927.1:p.Arg985=
ENST00000375365.2:c.2368_2369delinsCG	ENSP00000364514.2:p.Arg790=
ENST00000396435.7:c.2983_2984delinsCG	ENSP00000379712.3:p.Arg995=
NM_001111125.2:c.2983_2984delinsCG	NP_001104595.1:p.Arg995=
NM_015075.1:c.2368_2369delinsCG	NP_055890.1:p.Arg790=
XM_006724579.2:c.3079_3080delinsCG	XP_006724642.1:p.Arg1027=
XM_006724580.2:c.2368_2369delinsCG	XP_006724643.1:p.Arg790=
XM_006724581.2:c.3079_3080delinsCG	XP_006724644.1:p.Arg1027=
XM_006724582.2:c.3079_3080delinsCG	XP_006724645.1:p.Arg1027=
XM_006724583.2:c.3079_3080delinsCG	XP_006724646.1:p.Arg1027=
XM_006724584.2:c.3079_3080delinsCG	XP_006724647.1:p.Arg1027=
XM_011530772.1:c.2305_2306delinsCG	XP_011529074.1:p.Arg769=
XM_011530773.1:c.2272_2273delinsCG	XP_011529075.1:p.Arg758=
XM_011530774.1:c.3079_3080delinsCG	XP_011529076.1:p.Arg1027=
XM_011530775.1:c.3079_3080delinsCG	XP_011529077.1:p.Arg1027=
XM_011530776.1:c.3079_3080delinsCG	XP_011529078.1:p.Arg1027=
XM_011530777.1:c.3079_3080delinsCG	XP_011529079.1:p.Arg1027=
XR_938365.1:n.3306_3307delinsCG
XM_006724579.3:c.3079_3080delinsCG	XP_006724642.1:p.Arg1027=
XM_006724580.3:c.2368_2369delinsCG	XP_006724643.1:p.Arg790=
XM_006724581.4:c.3079_3080delinsCG	XP_006724644.1:p.Arg1027=
XM_006724582.4:c.3079_3080delinsCG	XP_006724645.1:p.Arg1027=
XM_006724583.4:c.3079_3080delinsCG	XP_006724646.1:p.Arg1027=
XM_006724584.3:c.3079_3080delinsCG	XP_006724647.1:p.Arg1027=
XM_011530773.2:c.2272_2273delinsCG	XP_011529075.1:p.Arg758=
XM_011530774.3:c.3079_3080delinsCG	XP_011529076.1:p.Arg1027=
XM_011530776.2:c.3079_3080delinsCG	XP_011529078.1:p.Arg1027=
XM_011530777.2:c.3079_3080delinsCG	XP_011529079.1:p.Arg1027=
XM_017029359.2:c.2953_2954delinsCG	XP_016884848.1:p.Arg985=
XM_017029360.1:c.2485_2486delinsCG	XP_016884849.1:p.Arg829=
XR_938365.2:n.3300_3301delinsCG
NM_001111125.3:c.2983_2984delinsCG MANE Select	NP_001104595.1:p.Arg995=
NM_015075.2:c.2368_2369delinsCG	NP_055890.1:p.Arg790=