Canonical Allele Identifier: CA2429775611
Gene: IQSEC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53250687C= , CM000685.2:g.53250687C= GRCh38
NC_000023.10:g.53279869C= , CM000685.1:g.53279869C= GRCh37
NC_000023.9:g.53296594C= NCBI36
NG_021296.1:g.75654G=
NG_021296.2:g.75664G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706952.1:c.2048G= ENSP00000516672.1:p.Gly683=
ENST00000640694.1:c.1889G= ENSP00000492403.1:p.Gly630=
ENST00000642864.1:c.1889G= MANE Select ENSP00000495726.1:p.Gly630=
ENST00000674510.1:c.1889G= ENSP00000502054.1:p.Gly630=
ENST00000675719.1:c.1859G= ENSP00000501927.1:p.Gly620=
ENST00000375365.2:c.1274G= ENSP00000364514.2:p.Gly425=
ENST00000396435.7:c.1889G= ENSP00000379712.3:p.Gly630=
NM_001111125.2:c.1889G= NP_001104595.1:p.Gly630=
NM_015075.1:c.1274G= NP_055890.1:p.Gly425=
XM_006724579.2:c.1985G= XP_006724642.1:p.Gly662=
XM_006724580.2:c.1274G= XP_006724643.1:p.Gly425=
XM_006724581.2:c.1985G= XP_006724644.1:p.Gly662=
XM_006724582.2:c.1985G= XP_006724645.1:p.Gly662=
XM_006724583.2:c.1985G= XP_006724646.1:p.Gly662=
XM_006724584.2:c.1985G= XP_006724647.1:p.Gly662=
XM_011530772.1:c.1211G= XP_011529074.1:p.Gly404=
XM_011530773.1:c.1178G= XP_011529075.1:p.Gly393=
XM_011530774.1:c.1985G= XP_011529076.1:p.Gly662=
XM_011530775.1:c.1985G= XP_011529077.1:p.Gly662=
XM_011530776.1:c.1985G= XP_011529078.1:p.Gly662=
XM_011530777.1:c.1985G= XP_011529079.1:p.Gly662=
XR_938365.1:n.2212G=
XM_006724579.3:c.1985G= XP_006724642.1:p.Gly662=
XM_006724580.3:c.1274G= XP_006724643.1:p.Gly425=
XM_006724581.4:c.1985G= XP_006724644.1:p.Gly662=
XM_006724582.4:c.1985G= XP_006724645.1:p.Gly662=
XM_006724583.4:c.1985G= XP_006724646.1:p.Gly662=
XM_006724584.3:c.1985G= XP_006724647.1:p.Gly662=
XM_011530773.2:c.1178G= XP_011529075.1:p.Gly393=
XM_011530774.3:c.1985G= XP_011529076.1:p.Gly662=
XM_011530776.2:c.1985G= XP_011529078.1:p.Gly662=
XM_011530777.2:c.1985G= XP_011529079.1:p.Gly662=
XM_017029359.2:c.1859G= XP_016884848.1:p.Gly620=
XM_017029360.1:c.1391G= XP_016884849.1:p.Gly464=
XR_938365.2:n.2206G=
NM_001111125.3:c.1889G= MANE Select NP_001104595.1:p.Gly630=
NM_015075.2:c.1274G= NP_055890.1:p.Gly425=