Canonical Allele Identifier: CA2956522098

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53241877_53241879del , CM000685.2:g.53241877_53241879del	GRCh38
NC_000023.10:g.53271059_53271061del , CM000685.1:g.53271059_53271061del	GRCh37
NC_000023.9:g.53287784_53287786del	NCBI36
NG_021296.1:g.84468_84470del
NG_021296.2:g.84478_84480del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3085_3087del	ENSP00000516672.1:p.Cys1029del
ENST00000638521.1:c.878_880del
ENST00000638869.1:c.387_389del
ENST00000639642.1:c.216_218del
ENST00000640694.1:c.2926_2928del	ENSP00000492403.1:p.Cys976del
ENST00000642864.1:c.2926_2928del MANE Select	ENSP00000495726.1:p.Cys976del
ENST00000674510.1:c.2926_2928del	ENSP00000502054.1:p.Cys976del
ENST00000674761.1:n.1233_1235del
ENST00000675719.1:c.2896_2898del	ENSP00000501927.1:p.Cys966del
ENST00000375365.2:c.2311_2313del	ENSP00000364514.2:p.Cys771del
ENST00000396435.7:c.2926_2928del	ENSP00000379712.3:p.Cys976del
NM_001111125.2:c.2926_2928del	NP_001104595.1:p.Cys976del
NM_015075.1:c.2311_2313del	NP_055890.1:p.Cys771del
XM_006724579.2:c.3022_3024del	XP_006724642.1:p.Cys1008del
XM_006724580.2:c.2311_2313del	XP_006724643.1:p.Cys771del
XM_006724581.2:c.3022_3024del	XP_006724644.1:p.Cys1008del
XM_006724582.2:c.3022_3024del	XP_006724645.1:p.Cys1008del
XM_006724583.2:c.3022_3024del	XP_006724646.1:p.Cys1008del
XM_006724584.2:c.3022_3024del	XP_006724647.1:p.Cys1008del
XM_011530772.1:c.2248_2250del	XP_011529074.1:p.Cys750del
XM_011530773.1:c.2215_2217del	XP_011529075.1:p.Cys739del
XM_011530774.1:c.3022_3024del	XP_011529076.1:p.Cys1008del
XM_011530775.1:c.3022_3024del	XP_011529077.1:p.Cys1008del
XM_011530776.1:c.3022_3024del	XP_011529078.1:p.Cys1008del
XM_011530777.1:c.3022_3024del	XP_011529079.1:p.Cys1008del
XR_938365.1:n.3249_3251del
XM_006724579.3:c.3022_3024del	XP_006724642.1:p.Cys1008del
XM_006724580.3:c.2311_2313del	XP_006724643.1:p.Cys771del
XM_006724581.4:c.3022_3024del	XP_006724644.1:p.Cys1008del
XM_006724582.4:c.3022_3024del	XP_006724645.1:p.Cys1008del
XM_006724583.4:c.3022_3024del	XP_006724646.1:p.Cys1008del
XM_006724584.3:c.3022_3024del	XP_006724647.1:p.Cys1008del
XM_011530773.2:c.2215_2217del	XP_011529075.1:p.Cys739del
XM_011530774.3:c.3022_3024del	XP_011529076.1:p.Cys1008del
XM_011530776.2:c.3022_3024del	XP_011529078.1:p.Cys1008del
XM_011530777.2:c.3022_3024del	XP_011529079.1:p.Cys1008del
XM_017029359.2:c.2896_2898del	XP_016884848.1:p.Cys966del
XM_017029360.1:c.2428_2430del	XP_016884849.1:p.Cys810del
XR_938365.2:n.3243_3245del
NM_001111125.3:c.2926_2928del MANE Select	NP_001104595.1:p.Cys976del
NM_015075.2:c.2311_2313del	NP_055890.1:p.Cys771del