Canonical Allele Identifier: CA2429770742
Gene: IQSEC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53235249_53235250delinsAC , CM000685.2:g.53235249_53235250delinsAC GRCh38
NC_000023.10:g.53264431_53264432delinsAC , CM000685.1:g.53264431_53264432delinsAC GRCh37
NC_000023.9:g.53281156_53281157delinsAC NCBI36
NG_021296.1:g.91091_91092delinsGT
NG_021296.2:g.91101_91102delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706952.1:c.3661-66_3661-65delinsGT ENSP00000516672.1:n.3661-66_3661-65delinsGT
ENST00000638521.1:c.1453+533_1453+534delinsGT
ENST00000638869.1:c.962+533_962+534delinsGT
ENST00000639796.1:c.316+1072_316+1073delinsGT ENSP00000492252.1:n.316+1072_316+1073delinsGT
ENST00000640005.1:c.514+1072_514+1073delinsGT ENSP00000491293.1:n.514+1072_514+1073delinsGT
ENST00000640436.1:n.482-66_482-65delinsGT
ENST00000640694.1:c.3452-66_3452-65delinsGT ENSP00000492403.1:n.3452-66_3452-65delinsGT
ENST00000642864.1:c.3502-66_3502-65delinsGT MANE Select ENSP00000495726.1:n.3502-66_3502-65delinsGT
ENST00000674510.1:c.3502-66_3502-65delinsGT ENSP00000502054.1:n.3502-66_3502-65delinsGT
ENST00000675719.1:c.3472-66_3472-65delinsGT ENSP00000501927.1:n.3472-66_3472-65delinsGT
ENST00000375365.2:c.2837-66_2837-65delinsGT ENSP00000364514.2:n.2837-66_2837-65delinsGT
ENST00000396435.7:c.3502-66_3502-65delinsGT ENSP00000379712.3:n.3502-66_3502-65delinsGT
NM_001111125.2:c.3502-66_3502-65delinsGT NP_001104595.1:n.3502-66_3502-65delinsGT
NM_015075.1:c.2837-66_2837-65delinsGT NP_055890.1:n.2837-66_2837-65delinsGT
XM_006724579.2:c.3598-66_3598-65delinsGT XP_006724642.1:n.3598-66_3598-65delinsGT
XM_006724580.2:c.2887-66_2887-65delinsGT XP_006724643.1:n.2887-66_2887-65delinsGT
XM_006724581.2:c.3597+533_3597+534delinsGT XP_006724644.1:n.3597+533_3597+534delinsGT
XM_006724582.2:c.3597+533_3597+534delinsGT XP_006724645.1:n.3597+533_3597+534delinsGT
XM_006724583.2:c.3547+1072_3547+1073delinsGT XP_006724646.1:n.3547+1072_3547+1073delinsGT
XM_006724584.2:c.3548-66_3548-65delinsGT XP_006724647.1:n.3548-66_3548-65delinsGT
XM_011530772.1:c.2824-66_2824-65delinsGT XP_011529074.1:n.2824-66_2824-65delinsGT
XM_011530773.1:c.2791-66_2791-65delinsGT XP_011529075.1:n.2791-66_2791-65delinsGT
XM_011530774.1:c.*237_*238delinsGT XP_011529076.1:n.*237_*238delinsGT
XM_011530775.1:c.3547+1072_3547+1073delinsGT XP_011529077.1:n.3547+1072_3547+1073delinsGT
XM_006724579.3:c.3598-66_3598-65delinsGT XP_006724642.1:n.3598-66_3598-65delinsGT
XM_006724580.3:c.2887-66_2887-65delinsGT XP_006724643.1:n.2887-66_2887-65delinsGT
XM_006724581.4:c.3597+533_3597+534delinsGT XP_006724644.1:n.3597+533_3597+534delinsGT
XM_006724582.4:c.3597+533_3597+534delinsGT XP_006724645.1:n.3597+533_3597+534delinsGT
XM_006724583.4:c.3547+1072_3547+1073delinsGT XP_006724646.1:n.3547+1072_3547+1073delinsGT
XM_006724584.3:c.3548-66_3548-65delinsGT XP_006724647.1:n.3548-66_3548-65delinsGT
XM_011530773.2:c.2791-66_2791-65delinsGT XP_011529075.1:n.2791-66_2791-65delinsGT
XM_011530774.3:c.*237_*238delinsGT XP_011529076.1:n.*237_*238delinsGT
XM_017029359.2:c.3472-66_3472-65delinsGT XP_016884848.1:n.3472-66_3472-65delinsGT
XM_017029360.1:c.3004-66_3004-65delinsGT XP_016884849.1:n.3004-66_3004-65delinsGT
NM_001111125.3:c.3502-66_3502-65delinsGT MANE Select NP_001104595.1:n.3502-66_3502-65delinsGT
NM_015075.2:c.2837-66_2837-65delinsGT NP_055890.1:n.2837-66_2837-65delinsGT