Canonical Allele Identifier: CA2739290487

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53243331_53243332insAATTGT , CM000685.2:g.53243331_53243332insAATTGT	GRCh38
NC_000023.10:g.53272513_53272514insAATTGT , CM000685.1:g.53272513_53272514insAATTGT	GRCh37
NC_000023.9:g.53289238_53289239insAATTGT	NCBI36
NG_021296.1:g.83009_83010insACAATT
NG_021296.2:g.83019_83020insACAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3048_3048+1insACAATT	ENSP00000516672.1:n.3048_3048+1insACAATT
ENST00000638521.1:c.841_841+1insACAATT
ENST00000638869.1:c.350_350+1insACAATT
ENST00000639642.1:c.179_179+1insACAATT
ENST00000640694.1:c.2889_2889+1insACAATT	ENSP00000492403.1:n.2889_2889+1insACAATT
ENST00000642864.1:c.2889_2889+1insACAATT MANE Select	ENSP00000495726.1:n.2889_2889+1insACAATT
ENST00000674510.1:c.2889_2889+1insACAATT	ENSP00000502054.1:n.2889_2889+1insACAATT
ENST00000674761.1:n.640_641insACAATT
ENST00000675719.1:c.2859_2859+1insACAATT	ENSP00000501927.1:n.2859_2859+1insACAATT
ENST00000375365.2:c.2274_2274+1insACAATT	ENSP00000364514.2:n.2274_2274+1insACAATT
ENST00000396435.7:c.2889_2889+1insACAATT	ENSP00000379712.3:n.2889_2889+1insACAATT
NM_001111125.2:c.2889_2889+1insACAATT	NP_001104595.1:n.2889_2889+1insACAATT
NM_015075.1:c.2274_2274+1insACAATT	NP_055890.1:n.2274_2274+1insACAATT
XM_006724579.2:c.2985_2985+1insACAATT	XP_006724642.1:n.2985_2985+1insACAATT
XM_006724580.2:c.2274_2274+1insACAATT	XP_006724643.1:n.2274_2274+1insACAATT
XM_006724581.2:c.2985_2985+1insACAATT	XP_006724644.1:n.2985_2985+1insACAATT
XM_006724582.2:c.2985_2985+1insACAATT	XP_006724645.1:n.2985_2985+1insACAATT
XM_006724583.2:c.2985_2985+1insACAATT	XP_006724646.1:n.2985_2985+1insACAATT
XM_006724584.2:c.2985_2985+1insACAATT	XP_006724647.1:n.2985_2985+1insACAATT
XM_011530772.1:c.2211_2211+1insACAATT	XP_011529074.1:n.2211_2211+1insACAATT
XM_011530773.1:c.2178_2178+1insACAATT	XP_011529075.1:n.2178_2178+1insACAATT
XM_011530774.1:c.2985_2985+1insACAATT	XP_011529076.1:n.2985_2985+1insACAATT
XM_011530775.1:c.2985_2985+1insACAATT	XP_011529077.1:n.2985_2985+1insACAATT
XM_011530776.1:c.2985_2985+1insACAATT	XP_011529078.1:n.2985_2985+1insACAATT
XM_011530777.1:c.2985_2985+1insACAATT	XP_011529079.1:n.2985_2985+1insACAATT
XR_938365.1:n.3212_3212+1insACAATT
XM_006724579.3:c.2985_2985+1insACAATT	XP_006724642.1:n.2985_2985+1insACAATT
XM_006724580.3:c.2274_2274+1insACAATT	XP_006724643.1:n.2274_2274+1insACAATT
XM_006724581.4:c.2985_2985+1insACAATT	XP_006724644.1:n.2985_2985+1insACAATT
XM_006724582.4:c.2985_2985+1insACAATT	XP_006724645.1:n.2985_2985+1insACAATT
XM_006724583.4:c.2985_2985+1insACAATT	XP_006724646.1:n.2985_2985+1insACAATT
XM_006724584.3:c.2985_2985+1insACAATT	XP_006724647.1:n.2985_2985+1insACAATT
XM_011530773.2:c.2178_2178+1insACAATT	XP_011529075.1:n.2178_2178+1insACAATT
XM_011530774.3:c.2985_2985+1insACAATT	XP_011529076.1:n.2985_2985+1insACAATT
XM_011530776.2:c.2985_2985+1insACAATT	XP_011529078.1:n.2985_2985+1insACAATT
XM_011530777.2:c.2985_2985+1insACAATT	XP_011529079.1:n.2985_2985+1insACAATT
XM_017029359.2:c.2859_2859+1insACAATT	XP_016884848.1:n.2859_2859+1insACAATT
XM_017029360.1:c.2391_2391+1insACAATT	XP_016884849.1:n.2391_2391+1insACAATT
XR_938365.2:n.3206_3206+1insACAATT
NM_001111125.3:c.2889_2889+1insACAATT MANE Select	NP_001104595.1:n.2889_2889+1insACAATT
NM_015075.2:c.2274_2274+1insACAATT	NP_055890.1:n.2274_2274+1insACAATT