Canonical Allele Identifier: CA2843144653
Gene: IQSEC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53241769_53241770del , CM000685.2:g.53241769_53241770del GRCh38
NC_000023.10:g.53270951_53270952del , CM000685.1:g.53270951_53270952del GRCh37
NC_000023.9:g.53287676_53287677del NCBI36
NG_021296.1:g.84574_84575del
NG_021296.2:g.84584_84585del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706952.1:c.3174+17_3174+18del ENSP00000516672.1:n.3174+17_3174+18del
ENST00000638521.1:c.967+17_967+18del
ENST00000638869.1:c.476+17_476+18del
ENST00000639642.1:c.305+17_305+18del
ENST00000640005.1:c.78+17_78+18del ENSP00000491293.1:n.78+17_78+18del
ENST00000640694.1:c.3015+17_3015+18del ENSP00000492403.1:n.3015+17_3015+18del
ENST00000642864.1:c.3015+17_3015+18del MANE Select ENSP00000495726.1:n.3015+17_3015+18del
ENST00000674510.1:c.3015+17_3015+18del ENSP00000502054.1:n.3015+17_3015+18del
ENST00000674761.1:n.1339_1340del
ENST00000675719.1:c.2985+17_2985+18del ENSP00000501927.1:n.2985+17_2985+18del
ENST00000375365.2:c.2400+17_2400+18del ENSP00000364514.2:n.2400+17_2400+18del
ENST00000396435.7:c.3015+17_3015+18del ENSP00000379712.3:n.3015+17_3015+18del
NM_001111125.2:c.3015+17_3015+18del NP_001104595.1:n.3015+17_3015+18del
NM_015075.1:c.2400+17_2400+18del NP_055890.1:n.2400+17_2400+18del
XM_006724579.2:c.3111+17_3111+18del XP_006724642.1:n.3111+17_3111+18del
XM_006724580.2:c.2400+17_2400+18del XP_006724643.1:n.2400+17_2400+18del
XM_006724581.2:c.3111+17_3111+18del XP_006724644.1:n.3111+17_3111+18del
XM_006724582.2:c.3111+17_3111+18del XP_006724645.1:n.3111+17_3111+18del
XM_006724583.2:c.3111+17_3111+18del XP_006724646.1:n.3111+17_3111+18del
XM_006724584.2:c.3111+17_3111+18del XP_006724647.1:n.3111+17_3111+18del
XM_011530772.1:c.2337+17_2337+18del XP_011529074.1:n.2337+17_2337+18del
XM_011530773.1:c.2304+17_2304+18del XP_011529075.1:n.2304+17_2304+18del
XM_011530774.1:c.3111+17_3111+18del XP_011529076.1:n.3111+17_3111+18del
XM_011530775.1:c.3111+17_3111+18del XP_011529077.1:n.3111+17_3111+18del
XM_011530776.1:c.3111+17_3111+18del XP_011529078.1:n.3111+17_3111+18del
XM_011530777.1:c.3111+17_3111+18del XP_011529079.1:n.3111+17_3111+18del
XR_938365.1:n.3338+17_3338+18del
XM_006724579.3:c.3111+17_3111+18del XP_006724642.1:n.3111+17_3111+18del
XM_006724580.3:c.2400+17_2400+18del XP_006724643.1:n.2400+17_2400+18del
XM_006724581.4:c.3111+17_3111+18del XP_006724644.1:n.3111+17_3111+18del
XM_006724582.4:c.3111+17_3111+18del XP_006724645.1:n.3111+17_3111+18del
XM_006724583.4:c.3111+17_3111+18del XP_006724646.1:n.3111+17_3111+18del
XM_006724584.3:c.3111+17_3111+18del XP_006724647.1:n.3111+17_3111+18del
XM_011530773.2:c.2304+17_2304+18del XP_011529075.1:n.2304+17_2304+18del
XM_011530774.3:c.3111+17_3111+18del XP_011529076.1:n.3111+17_3111+18del
XM_011530776.2:c.3111+17_3111+18del XP_011529078.1:n.3111+17_3111+18del
XM_011530777.2:c.3111+17_3111+18del XP_011529079.1:n.3111+17_3111+18del
XM_017029359.2:c.2985+17_2985+18del XP_016884848.1:n.2985+17_2985+18del
XM_017029360.1:c.2517+17_2517+18del XP_016884849.1:n.2517+17_2517+18del
XR_938365.2:n.3332+17_3332+18del
NM_001111125.3:c.3015+17_3015+18del MANE Select NP_001104595.1:n.3015+17_3015+18del
NM_015075.2:c.2400+17_2400+18del NP_055890.1:n.2400+17_2400+18del